(2S)-hydroxysuccinic acid-1-benzyl ester-4-(4-methoxybenzyl) ester

Base Information

• Chemical Name: (2S)-hydroxysuccinic acid-1-benzyl ester-4-(4-methoxybenzyl) ester
• CAS No.: 260408-09-1
• Molecular Formula: C₁₉H₂₀O₆
• Molecular Weight: 344.364
• Mol file: 260408-09-1.mol

Synonyms:(2S)-hydroxysuccinic acid-1-benzyl ester-4-(4-methoxybenzyl) ester

Chemical Property of (2S)-hydroxysuccinic acid-1-benzyl ester-4-(4-methoxybenzyl) ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2S)-hydroxysuccinic acid-1-benzyl ester-4-(4-methoxybenzyl) ester

There total 3 articles about (2S)-hydroxysuccinic acid-1-benzyl ester-4-(4-methoxybenzyl) 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: 74.0%

(S)-3-(Benzyloxycarbonyl)-3-hydroxypropanoic acid (66178-04-9) + p-methoxybenzyl chloride (824-94-2) → (2S)-hydroxysuccinic acid-1-benzyl ester-4-(4-methoxybenzyl) ester (260408-09-1)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 96h;

DOI:10.1021/ol991264x

Reference yield:

benzyl alcohol (100-51-6,185532-71-2) → (2S)-hydroxysuccinic acid-1-benzyl ester-4-(4-methoxybenzyl) ester (260408-09-1)

Guidance literature:

Multi-step reaction with 2 steps

1.1: TFAA / 0 °C

1.2: 20 °C

2.1: K₃CO₃ / dimethylformamide / 96 h / 20 °C

With potassium carbonate; trifluoroacetic anhydride; In N,N-dimethyl-formamide;

DOI:10.1021/ja003770j

Reference yield:

benzyl alcohol (100-51-6,185532-71-2) → (2S)-hydroxysuccinic acid-1-benzyl ester-4-(4-methoxybenzyl) ester (260408-09-1)

Guidance literature:

Multi-step reaction with 2 steps

1.1: trifluoroacetic anhydride / 0 °C

1.2: 80 percent / 20 °C

2.1: 74 percent / K₂CO₃ / dimethylformamide / 96 h / 20 °C

With potassium carbonate; trifluoroacetic anhydride; In N,N-dimethyl-formamide; 1.1: Acylation / 1.2: Acylation / 2.1: Acylation;

DOI:10.1021/ol991264x

upstream raw materials:

(S)-3-(Benzyloxycarbonyl)-3-hydroxypropanoic acid

p-methoxybenzyl chloride

benzyl alcohol

Downstream raw materials:

(2R)-methanesulfanyl-succinic acid-1-benzyl ester-4-(4-methoxybenzyl) ester

N-[(2-S-benzyloxycarbonylamino-3-phenyl-propanoylamino)methyl] 2-R-methanesulfanyl succinamic acid benzyl ester

2-S-{[(3-benzyloxycarbonyl-3-R-methanesulfanyl-propanoyl-amino)methyl]carbamoyl}pyrrolidine-1-carboxylic acid benzyl ester

N-[(2-S-benzyloxycarbonylamino-3-methylpentanoylamino)methyl] 2-R-methanesulfanyl succinamic benzyl ester