(-)-(1S,2S)-2-[(tert-Butoxycarbonyl)amino]-1-phenyl-1,3-propandiylbis[4-(chlormethyl)benzoat]

Base Information

• Chemical Name: (-)-(1S,2S)-2-[(tert-Butoxycarbonyl)amino]-1-phenyl-1,3-propandiylbis[4-(chlormethyl)benzoat]
• CAS No.: 167082-58-8
• Molecular Formula: C₃₀H₃₁Cl₂NO₆
• Molecular Weight: 572.485
• Mol file: 167082-58-8.mol

Synonyms:(-)-(1S,2S)-2-[(tert-Butoxycarbonyl)amino]-1-phenyl-1,3-propandiylbis[4-(chlormethyl)benzoat]

Chemical Property of (-)-(1S,2S)-2-[(tert-Butoxycarbonyl)amino]-1-phenyl-1,3-propandiylbis[4-(chlormethyl)benzoat]

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (-)-(1S,2S)-2-[(tert-Butoxycarbonyl)amino]-1-phenyl-1,3-propandiylbis[4-(chlormethyl)benzoat]

There total 3 articles about (-)-(1S,2S)-2-[(tert-Butoxycarbonyl)amino]-1-phenyl-1,3-propandiylbis[4-(chlormethyl)benzoat] 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: 85.0%

p-(chloromethyl)benzoyl chloride (876-08-4) + tert-butyl [(1S,2S)-1,3-dihydroxy-1-phenylpropan-2-yl]carbamate (167082-56-6) → (-)-(1S,2S)-2-[(tert-Butoxycarbonyl)amino]-1-phenyl-1,3-propandiylbis[4-(chlormethyl)benzoat] (167082-58-8)

Guidance literature:

With pyridine; In dichloromethane; 1.) 0 deg C, 1 h, 2.) r.t., 6 h;

Reference yield:

di-tert-butyl dicarbonate (24424-99-5) → (-)-(1S,2S)-2-[(tert-Butoxycarbonyl)amino]-1-phenyl-1,3-propandiylbis[4-(chlormethyl)benzoat] (167082-58-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 89 percent / methanol / 0.5 h / Ambient temperature

2: 85 percent / pyridine / CH₂Cl₂ / 1.) 0 deg C, 1 h, 2.) r.t., 6 h

With pyridine; In methanol; dichloromethane;

Reference yield:

(1S,2S)-2-amino-1-phenyl-1,3-diol (28143-91-1) → (-)-(1S,2S)-2-[(tert-Butoxycarbonyl)amino]-1-phenyl-1,3-propandiylbis[4-(chlormethyl)benzoat] (167082-58-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 89 percent / methanol / 0.5 h / Ambient temperature

2: 85 percent / pyridine / CH₂Cl₂ / 1.) 0 deg C, 1 h, 2.) r.t., 6 h

With pyridine; In methanol; dichloromethane;

upstream raw materials:

p-(chloromethyl)benzoyl chloride

tert-butyl [(1S,2S)-1,3-dihydroxy-1-phenylpropan-2-yl]carbamate

di-tert-butyl dicarbonate

(1S,2S)-2-amino-1-phenyl-1,3-diol

Downstream raw materials:

(1S,2S)-2-N-tert-Butyloxycarbonyl-amino-1-phenyl-1,3-propandiyl-bis[4-(N-methyl-N-(R)-1-phenylethyl)aminomethylbenzoat]