{(1R,2R)-2-Benzyloxy-1-[(methoxy-methyl-carbamoyl)-methyl]-propyl}-carbamic acid tert-butyl ester

Base Information

• Chemical Name: {(1R,2R)-2-Benzyloxy-1-[(methoxy-methyl-carbamoyl)-methyl]-propyl}-carbamic acid tert-butyl ester
• CAS No.: 210533-65-6
• Molecular Formula: C₁₉H₃₀N₂O₅
• Molecular Weight: 366.458
• Mol file: 210533-65-6.mol

Synonyms:{(1R,2R)-2-Benzyloxy-1-[(methoxy-methyl-carbamoyl)-methyl]-propyl}-carbamic acid tert-butyl ester

Chemical Property of {(1R,2R)-2-Benzyloxy-1-[(methoxy-methyl-carbamoyl)-methyl]-propyl}-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of {(1R,2R)-2-Benzyloxy-1-[(methoxy-methyl-carbamoyl)-methyl]-propyl}-carbamic acid tert-butyl ester

There total 4 articles about {(1R,2R)-2-Benzyloxy-1-[(methoxy-methyl-carbamoyl)-methyl]-propyl}-carbamic acid tert-butyl 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: 84.0%

tert-butyl N-{(1S)-3-diazo-1-[(1R)-1-(benzyloxy)ethyl]-2-oxopropyl}carbamate (210533-59-8) + N,0-dimethylhydroxylamine (1117-97-1) → {(1R,2R)-2-Benzyloxy-1-[(methoxy-methyl-carbamoyl)-methyl]-propyl}-carbamic acid tert-butyl ester (210533-65-6)

Guidance literature:

With silver benzoate; triethylamine; In tetrahydrofuran; at -25 - 20 ℃; for 2h;

DOI:10.1016/S0040-4039(98)00675-3

Reference yield:

((2R,3R)-3-benzyloxy-2-t-butoxycarbonyl-aminobutoxy)acetic acid (1004791-12-1) + N,O-dimethylhydroxylamine*hydrochloride (6638-79-5) → {(1R,2R)-2-Benzyloxy-1-[(methoxy-methyl-carbamoyl)-methyl]-propyl}-carbamic acid tert-butyl ester (210533-65-6)

Guidance literature:

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 16h;

Reference yield:

N-Boc-O-benzyl-L-threonine (15260-10-3) → {(1R,2R)-2-Benzyloxy-1-[(methoxy-methyl-carbamoyl)-methyl]-propyl}-carbamic acid tert-butyl ester (210533-65-6)

Guidance literature:

Multi-step reaction with 3 steps

1: NMM / tetrahydrofuran / 1 h / -25 °C

2: diethyl ether / 2 h / Ambient temperature

3: 84 percent / Et₃N, C₆H₅CO₂Ag / tetrahydrofuran / 2 h / -25 - 20 °C

With 4-methyl-morpholine; silver benzoate; triethylamine; In tetrahydrofuran; diethyl ether;

DOI:10.1016/S0040-4039(98)00675-3

upstream raw materials:

tert-butyl N-{(1S)-3-diazo-1-[(1R)-1-(benzyloxy)ethyl]-2-oxopropyl}carbamate

N,0-dimethylhydroxylamine

N-Boc-O-benzyl-L-threonine

C₂₁H₃₁NO₇

Downstream raw materials:

{(1R,2R)-2-benzyloxy-1-[2-(4-chlorophenyl)-2-oxoethoxymethyl]propyl}carbamic acid t-butyl ester