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305329-97-9

305329-97-9 Structure

305329-97-9 Structure
IdentificationBack Directory
[Name]

tert-Butyl 3-(bromomethyl)pyrrolidine-1-carboxylate
[CAS]

305329-97-9
[Synonyms]

N-Boc-3-Bromomethylpyrroline
Boc-3-Bromomethyl-pyrrolidine
N-BOC-3-BROMOMETHYLPYRROLIDINE
1-Boc-3-(broMoMethyl)pyrrolidine
1-N-Boc-3-broMoMethylpyrrolidine
REF DUPL: Boc-3-Bromomethyl-pyrrolidine
t-butyl-3-(bromomethyl)pyrrolidine-1-carboxylate
tert-butyl 3-(brommethyl)pyrrolidine-1-carboxylate
TERT-BUTYL 3-(BROMOMETHYL)PYRROLIDINE-1-CARBOXYLATE
3-BROMOMETHYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
tert-Butyl 3-(bromomethyl)pyrrolidine-1-carboxylate≥ 95% (GC)
1-Pyrrolidinecarboxylic acid, 3-(bromomethyl)-, 1,1-dimethylethyl ester
[Molecular Formula]

C10H18BrNO2
[MDL Number]

MFCD06410515
[MOL File]

305329-97-9.mol
[Molecular Weight]

264.16
Chemical PropertiesBack Directory
[Boiling point ]

300.1±15.0 °C(Predicted)
[density ]

1.312±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

-2.14±0.40(Predicted)
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302+H312-H314
[Precautionary statements ]

P260-P264-P270-P280-P301+P312+P330-P301+P330+P331-P303+P361+P353-P304+P340+P310-P305+P351+P338+P310-P362+P364-P405-P501
[Hazard Codes ]

Xn
[Risk Statements ]

22
[HazardClass ]

IRRITANT
[HS Code ]

2933998090
Hazard InformationBack Directory
[Chemical Properties]

Liquid
[Synthesis]

1-Boc-3-hydroxymethylpyrrolidine

114214-69-6

tert-Butyl 3-(bromomethyl)pyrrolidine-1-carboxylate

305329-97-9

The general procedure for the synthesis of 1-Boc-3-(bromomethyl)pyrrolidine from 1-Boc-3-hydroxymethylpyrrolidine was as follows: 1,1-dimethylethyl-3-(hydroxymethyl)-1-pyrrolidine carboxylate (0.56 g, 2.8 mmol) was dissolved in dichloromethane (10 mL) under the protection of nitrogen and carbon tribromide (1.39 g, 4.2 mmol) was added. Subsequently, a solution of triphenylphosphine (0.73 g, 2.8 mmol) in dichloromethane (5 mL) was added slowly and dropwise. After the dropwise addition, the reaction mixture was stirred at room temperature for 18 hours. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in a 10% ethyl acetate/90% hexane solvent mixture, stirred and filtered. The filtrate was purified by silica gel column chromatography using a gradient elution of 0-25% ethyl acetate/hexane, and the target fraction was collected to give 1-Boc-3-(bromomethyl)pyrrolidine (0.41 g, 55% yield). Mass spectrum (electrospray positive ion mode) m/z 264 ([M+H]+).

[References]

[1] Patent: WO2007/58850, 2007, A2. Location in patent: Page/Page column 52-53
[2] Journal of Medicinal Chemistry, 2008, vol. 51, # 18, p. 5663 - 5679
[3] Patent: WO2008/121685, 2008, A1. Location in patent: Page/Page column 46
[4] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 5, p. 1151 - 1175
Spectrum DetailBack Directory
[Spectrum Detail]

tert-Butyl 3-(bromomethyl)pyrrolidine-1-carboxylate(305329-97-9)1HNMR
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