(S)-3-(tert-butoxycarbonylamino)-4-(tert-butyldimethylsiloxy)butyric acid benzyl ester

Base Information

• Chemical Name: (S)-3-(tert-butoxycarbonylamino)-4-(tert-butyldimethylsiloxy)butyric acid benzyl ester
• CAS No.: 221106-60-1
• Molecular Formula: C₂₂H₃₇NO₅Si
• Molecular Weight: 423.625
• Mol file: 221106-60-1.mol

Synonyms:(S)-3-(tert-butoxycarbonylamino)-4-(tert-butyldimethylsiloxy)butyric acid benzyl ester

Chemical Property of (S)-3-(tert-butoxycarbonylamino)-4-(tert-butyldimethylsiloxy)butyric acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-3-(tert-butoxycarbonylamino)-4-(tert-butyldimethylsiloxy)butyric acid benzyl ester

There total 8 articles about (S)-3-(tert-butoxycarbonylamino)-4-(tert-butyldimethylsiloxy)butyric acid benzyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

benzyl (3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutanoate (79069-16-2) + tert-butyldimethylsilyl chloride (18162-48-6) → (S)-3-(tert-butoxycarbonylamino)-4-(tert-butyldimethylsiloxy)butyric acid benzyl ester (221106-60-1)

Guidance literature:

With 1H-imidazole; In N,N-dimethyl-formamide; for 6h; Ambient temperature;

DOI:10.1248/cpb.47.11

Reference yield:

benzyl bromide (100-39-0) + 3-tert-butoxycarbonylamino-4-(tert-butyl-dimethyl-silanyloxy)-butyric acid (911634-87-2) → (S)-3-(tert-butoxycarbonylamino)-4-(tert-butyldimethylsiloxy)butyric acid benzyl ester (221106-60-1)

Guidance literature:

With triethylamine; In acetone; at 20 ℃; for 16h;

DOI:10.1055/s-2003-38733

Reference yield:

BOC-L-aspartic acid 4-benzyl ester (7536-58-5,98482-77-0) → (S)-3-(tert-butoxycarbonylamino)-4-(tert-butyldimethylsiloxy)butyric acid benzyl ester (221106-60-1)

Guidance literature:

Multi-step reaction with 3 steps

1: NMM / 1,2-dimethoxy-ethane / 0.5 h / -15 °C

2: aq. NaBH₄ / -50 - -15 °C

3: 90 percent / Et₃N; DMAP / CH₂Cl₂ / 20 °C

With 4-methyl-morpholine; dmap; sodium tetrahydroborate; triethylamine; In 1,2-dimethoxyethane; dichloromethane;

DOI:10.1055/s-2005-868494

upstream raw materials:

benzyl (3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutanoate

tert-butyldimethylsilyl chloride

benzyl bromide

3-tert-butoxycarbonylamino-4-(tert-butyl-dimethyl-silanyloxy)-butyric acid