N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine
- CAS No.
- 93102-05-7
- Chemical Name:
- N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine
- Synonyms
- N-benzyl-1-methoxy-N-((trimethylsilyl)methyl)methanamine;N-(MethoxyMethyl)-1-phenyl-N-(triMethylsilylMethyl)MethanaMine;N-benzyl(methoxy)-N-((trimethylsilyl)methyl)methanamine;)-N-trimethyL;cas:93102-05-7;-N-(methoxymethyL;N-(Methoxymethyl)-N-(trimethyl;N-(Methoxymethyl)-N-(trimethylsilyl) benzylamine;Benzyl-methoxymethyl-trimethylsilanylmethylamine;N-Benzyl-N-methoxymethyltrimethylsilylmethanamine
- CBNumber:
- CB2715045
- Molecular Formula:
- C13H23NOSi
- Molecular Weight:
- 237.41
- MDL Number:
- MFCD00674005
- MOL File:
- 93102-05-7.mol
- MSDS File:
- SDS
Boiling point | 76 °C0.3 mm Hg(lit.) |
---|---|
Density | 0.928 g/mL at 25 °C(lit.) |
refractive index |
n |
Flash point | 151 °F |
storage temp. | Keep in dark place,Sealed in dry,Room Temperature |
solubility | Soluble in chloroform, ethyl acetate. |
form | Liquid |
pka | 7.29±0.50(Predicted) |
color | Clear colorless to light yellow |
Specific Gravity | 0.928 |
Sensitive | Moisture & Light Sensitive |
Hydrolytic Sensitivity | 2: reacts with aqueous acid |
BRN | 4311216 |
InChIKey | RPZAAFUKDPKTKP-UHFFFAOYSA-N |
CAS DataBase Reference | 93102-05-7(CAS DataBase Reference) |
SAFETY
Risk and Safety Statements
Symbol(GHS) | GHS07 |
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Signal word | Warning | |||||||||
Hazard statements | H315-H319-H335 | |||||||||
Precautionary statements | P261-P264-P271-P280-P302+P352-P305+P351+P338 | |||||||||
Hazard Codes | Xi | |||||||||
Risk Statements | 36/37/38 | |||||||||
Safety Statements | 26-37/39 | |||||||||
RIDADR | 1993 | |||||||||
WGK Germany | 3 | |||||||||
HazardClass | 3 | |||||||||
PackingGroup | Ⅲ | |||||||||
HS Code | 29319090 | |||||||||
NFPA 704 |
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N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine price More Price(49)
Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|---|
Sigma-Aldrich | 420697 | N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine 96% | 93102-05-7 | 5g | $16.64 | 2024-03-01 | Buy |
Sigma-Aldrich | 420697 | N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine 96% | 93102-05-7 | 25g | $136 | 2024-03-01 | Buy |
TCI Chemical | B1938 | N-Benzyl-N-(methoxymethyl)-N-trimethylsilylmethylamine >98.0%(T) | 93102-05-7 | 5g | $35 | 2024-03-01 | Buy |
TCI Chemical | B1938 | N-Benzyl-N-(methoxymethyl)-N-trimethylsilylmethylamine >98.0%(T) | 93102-05-7 | 25g | $140 | 2024-03-01 | Buy |
Alfa Aesar | L19412 | N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine, 94% | 93102-05-7 | 1g | $38.65 | 2024-03-01 | Buy |
N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine Chemical Properties,Uses,Production
Preparation
N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine is most conveniently prepared by treatment of benzylamine with chloromethyltrimethylsilane followed by formaldehyde and methanol. Access to higher ether homologs is achieved by replacing methanol with the appropriate alcohol. An alternate procedure involves alkylation of lithium N-benzyltrimethylsilymethylamide with methoxymethyl chloride.
Chemical Properties
N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine is clear colorless to light yellow liquid
Physical properties
bp 77–80°C/0.5 mmHg.
Uses
N-Benzyl-N-(methoxymethyl)- N-trimethylsilylmethylamine (1) is a valuable reagent for in situ generation of the N-benzyl azomethine ylide (2). It is generally preferred over alternative silylmethylamine precursors6–8 because of ease of handling and use. The ylide (2) is most conveniently generated from (1) using a catalytic amount of trifluoroacetic acid as described by Achiwa.Alternative catalysts include LiF, TBAF,Me3SiOTf–CsF, or Me3SiI–CsF. Mechanistic studies provide evidence that the reactive intermediate generated from (1) with either CF3CO2H or F? is a 1,3-dipolar species. Reaction of (2) with alkenes provides an efficient convergent route to pyrrolidine derivatives. Alkynes afford 3-pyrrolines which can be converted into pyrroles.The ylide (2) reacts most readily with electron deficient alkenes and alkynes since this pairing results in a narrow dipole HOMO–dipolarophile LUMO energy gap.Examples of suitable dipolarophiles include unsaturated esters, ketones, imides,nitriles,and sulfones. Cycloaddition occurs with complete cis stereospecificity (eq 1) which is consistent with a concerted mechanism. Dipolarophiles containing an endocyclic double bond afford fused bicyclic pyrrolidines, whereas substrates with an exocyclic double bond provide access to spirocyclic systems.
Uses
N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine is useful reagent in synthesizing N-benzyl substituted pyrrolidines by [3+2] cycloaddition to α,ßunsaturated esters.
Uses
N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine forms azomethine ylides which readily undergo [3+2] cycloaddition to α,?-unsaturated esters affording N-benzyl substituted pyrrolidines in good yields. It reacts with asymmetric 1,3-dipolar cycloadditions in the practical, large-scale synthesis of chiral pyrrolidines. It is used in the the synthesis of 3-carboxy-1-azabicyclo[2.2.1]heptane derivatives, an important class of physiologically active compounds.
Preparation
most conveniently prepared by treatment of benzylamine with chloromethyltrimethylsilane followed by formaldehyde and methanol.Access to higher ether homologs is achieved by replacing methanol with the appropriate alcohol. An alternate procedure involves alkylation of lithium N-benzyltrimethylsilymethylamide with methoxymethyl chloride.
N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine Preparation Products And Raw materials
Raw materials
Preparation Products
1of2
Supplier | Tel | Country | ProdList | Advantage | |
---|---|---|---|---|---|
SHANDONG OUCHEM CO.,LTD. | +86-18506360988 +86-18506360988 | wtaili@ouchem.cn | China | 48 | 58 |
Hebei Mojin Biotechnology Co.,Ltd | +86-15028179902 | angelia@hbmojin.com | China | 1069 | 58 |
Frapp's ChemicalNFTZ Co., Ltd. | +86 (576) 8169-6106 | sales@frappschem.com | China | 885 | 50 |
Capot Chemical Co.,Ltd. | 571-85586718 +8613336195806 | sales@capotchem.com | China | 29798 | 60 |
Shanghai Daken Advanced Materials Co.,Ltd | +86-371-66670886 | info@dakenam.com | China | 18628 | 58 |
Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 | info@tianfuchem.com | China | 21667 | 55 |
Hangzhou FandaChem Co.,Ltd. | 008657128800458; +8615858145714 | fandachem@gmail.com | China | 9357 | 55 |
Nanjing ChemLin Chemical Industry Co., Ltd. | 025-83697070 | product@chemlin.com.cn | CHINA | 3012 | 60 |
ATK CHEMICAL COMPANY LIMITED | +undefined-21-51877795 | ivan@atkchemical.com | China | 32836 | 60 |
AB PharmaTech,LLC | 323-480-4688 | United States | 989 | 55 |
Related articles
- Application of N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine
- N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine forms azomethine ylides which readily undergo[3+2] cycloaddition to α,?-un....
- Dec 31,2019
View Lastest Price from N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine manufacturers
Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
---|---|---|---|---|---|---|---|---|
2024-08-14 | N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine
93102-05-7
|
US $0.00 / kg | 1kg | 99% | 50000KG/month | Hebei Mojin Biotechnology Co.,Ltd | ||
2024-07-24 | N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine
93102-05-7
|
US $0.00-0.00 / KG | 600KG | 95% Min. | 5MT | SHANDONG OUCHEM CO.,LTD. | ||
2023-03-09 | N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine
93102-05-7
|
US $0.00-0.00 / KG | 1KG | 99% | 20 mt | Hebei Guanlang Biotechnology Co., Ltd. |
- N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine
93102-05-7
- US $0.00 / kg
- 99%
- Hebei Mojin Biotechnology Co.,Ltd
- N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine
93102-05-7
- US $0.00-0.00 / KG
- 95% Min.
- SHANDONG OUCHEM CO.,LTD.
- N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine
93102-05-7
- US $0.00-0.00 / KG
- 99%
- Hebei Guanlang Biotechnology Co., Ltd.