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15260-10-3

15260-10-3 Structure

15260-10-3 Structure
IdentificationMore
[Name]

Boc-O-Benzyl-L-threonine
[CAS]

15260-10-3
[Synonyms]

BOC-L-THR(BZL)
BOC-L-THR(BZL)-OH
BOC-L-THREONINE
BOC-L-THREONINE (BZL)
BOC-L-THREONINE-OH
BOC-L-THR-OH
BOC-O-BENZYL-L-THREONINE
BOC-THR(BZL)
BOC-THR(BZL)-OH
BOC-THREONINE
BOC-THREONINE(BZL)-OH
BOC-THR-OH
N-ALPHA-T-BOC-L-THREONINE
N-ALPHA-T-BOC-O-BENZYL-L-THREONINE
N-ALPHA-T-BUTOXYCARBONYL-L-THREONINE
N-ALPHA-T-BUTOXYCARBONYL-O-BENZYL-L-THREONINE
N-ALPHA-TERT-BOC-O-BENZYL-L-THREONINE
N-ALPHA-TERT-BUTYLOXYCARBONYL-L-THREONINE
N-ALPHA-TERT-BUTYLOXYCARBONYL-O-BENZYL-L-THREONINE
N-BOC-L-THREONINE
[EINECS(EC#)]

239-304-5
[Molecular Formula]

C16H23NO5
[MDL Number]

MFCD00065946
[Molecular Weight]

309.36
[MOL File]

15260-10-3.mol
Chemical PropertiesBack Directory
[Melting point ]

80-82 °C(lit.)
[alpha ]

22 º (c=2 in 95% ethanol)
[Boiling point ]

461.5±45.0 °C(Predicted)
[density ]

1.152±0.06 g/cm3(Predicted)
[refractive index ]

16.5 ° (C=1, MeOH)
[storage temp. ]

2-8°C
[solubility ]

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
[form ]

powder to crystal
[pka]

3.50±0.10(Predicted)
[color ]

White to Almost white
[Optical Rotation]

[α]20/D +16.5±1°, c = 1% in methanol
[BRN ]

3065591
[Major Application]

peptide synthesis
[InChI]

InChI=1S/C16H23NO5/c1-11(21-10-12-8-6-5-7-9-12)13(14(18)19)17-15(20)22-16(2,3)4/h5-9,11,13H,10H2,1-4H3,(H,17,20)(H,18,19)/t11-,13+/m1/s1
[InChIKey]

CTXPLTPDOISPTE-YPMHNXCESA-N
[SMILES]

C(O)(=O)[C@H]([C@H](OCC1=CC=CC=C1)C)NC(OC(C)(C)C)=O
[CAS DataBase Reference]

15260-10-3(CAS DataBase Reference)
[EPA Substance Registry System]

15260-10-3(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[TSCA ]

Yes
[HS Code ]

29242990
[Storage Class]

13 - Non Combustible Solids
Raw materials And Preparation ProductsBack Directory
[Raw materials]

1,4-Dioxane-->L-Threonine-->Boc-L-Threonine-->Benzyl bromide-->Mineral oil-->N,N-Dimethylformamide-->Sodium hydride
[Preparation Products]

Boc-L-Threonine-->H-Thr(Bzl)-OH
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

N-tert-Butoxycarbonyl-O-benzyl-L-threonine(15260-10-3).msds
Hazard InformationBack Directory
[Chemical Properties]

White crystalline
[Application]

Boc-Thr(Bzl)-OH is a standard building block for introduction of threonine amino-acid residues by Boc SPPS.
[Uses]

Boc-O-benzyl-L-threonine, is an amino acid building block used in peptide synthesis. With a growing peptide drug market the fast, reliable synthesis of peptides is of great importance.
[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
[Synthesis]

Boc-L-Threonine

2592-18-9

Benzyl bromide

100-39-0

Boc-Thr(Bzl)-OH

15260-10-3

To a stirred solution of (2S,3R)-2-((tert-butoxycarbonyl)amino)-3-hydroxybutanoic acid (250 g, 1.44 mol) in DMF (1 L) was added 60% sodium hydride (68 g, 2.85 mol) in batches at -20 °C and protected by nitrogen and stirring was continued for 2 hours. Subsequently, benzyl bromide (167 mL, 1.36 mol) was slowly added dropwise and the reaction mixture was continued to be stirred at room temperature for 3 hours. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming complete consumption of the raw materials, the reaction was quenched with ice water and subsequently washed with ether (2 x 250 mL). The aqueous layer was separated and the pH was adjusted to about 2 with citric acid solution, followed by extraction with ethyl acetate (2 x 300 mL). The organic layers were combined, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford (2S,3R)-3-(benzyloxy)-2-((tert-butoxycarbonyl)amino)butanoic acid (320 g, 90% yield) as a thick paste.1H-NMR (500 MHz, DMSO-d6) data: δ 12.64 (broad single peak, 1H), 7.34-7.25 (multiple peaks, 5H), and 6.46 (double peak, J=8.5Hz, 1H), 4.53 (double peak, J=11.5Hz, 1H), 4.39 (double peak, J=12.0Hz, 1H), 4.00-3.98 (multiple peaks, 2H), 1.39 (single peak, 9H), 1.15 (double peak, J=6.0Hz, 3H).

[References]

[1] Patent: WO2018/26763, 2018, A1. Location in patent: Page/Page column 63
[2] Patent: WO2014/120786, 2014, A1. Location in patent: Paragraph 0101
[3] Patent: WO2014/120783, 2014, A1. Location in patent: Paragraph 0093
[4] Patent: WO2017/195069, 2017, A1. Location in patent: Page/Page column 66
[5] Bulletin of the Chemical Society of Japan, 1995, vol. 68, # 5, p. 1369 - 1377
Spectrum DetailBack Directory
[Spectrum Detail]

Boc-O-Benzyl-L-threonine(15260-10-3)MS
Boc-O-Benzyl-L-threonine(15260-10-3)1HNMR
Boc-O-Benzyl-L-threonine(15260-10-3)13CNMR
Boc-O-Benzyl-L-threonine(15260-10-3)IR1
Boc-O-Benzyl-L-threonine(15260-10-3)IR2
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

N-Boc-O-benzyl-L-threonine, 99%(15260-10-3)
[Sigma Aldrich]

15260-10-3(sigmaaldrich)
[TCI AMERICA]

N-(tert-Butoxycarbonyl)-O-benzyl-L-threonine,>98.0%(T)(15260-10-3)
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