-S-benzyl-L-cysteine Benzyl Ester

Base Information

Chemical Name:-S-benzyl-L-cysteine Benzyl Ester
CAS No.:76499-09-7
Molecular Formula:C₃₂H₃₈N₂O₅S₂
Molecular Weight:594.796
Hs Code.:

<N-(Carbobenzoxy)-S-tert-butyl-L-cysteinyl>-S-benzyl-L-cysteine Benzyl Ester

Synonyms:-S-benzyl-L-cysteine Benzyl Ester

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Chemical Property of -S-benzyl-L-cysteine Benzyl Ester

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Technology Process of -S-benzyl-L-cysteine Benzyl Ester

There total 4 articles about -S-benzyl-L-cysteine 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: 78.0%

: 73995-16-1
S-benzylcysteine benzyl ester p-toluenesulfonate

: 2481-12-1
Dicyclohexylamine Salt of N-(Carbobenzoxy)-S-tert-butyl-L-cysteine

: 76499-09-7
-S-benzyl-L-cysteine Benzyl Ester

Guidance literature:: With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In tetrahydrofuran; for 8h; Ambient temperature;
DOI:10.1021/jo00322a024

Reference yield:

: 2481-09-6
S-tert-Butyl-N-acetyl-L-cysteine hydrochloride

: 76499-09-7
-S-benzyl-L-cysteine Benzyl Ester

Guidance literature:: Multi-step reaction with 2 steps

2: 78 percent / 2-Ethoxy-N-(ethoxycarbonyl)-1,2-dihydroquinoline (EEDQ) / tetrahydrofuran / 8 h / Ambient temperature

With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In tetrahydrofuran;
DOI:10.1021/jo00322a024

Reference yield:

: 501-53-1,94274-21-2
benzyl chloroformate

: 76499-09-7
-S-benzyl-L-cysteine Benzyl Ester

Guidance literature:: Multi-step reaction with 2 steps

2: 78 percent / 2-Ethoxy-N-(ethoxycarbonyl)-1,2-dihydroquinoline (EEDQ) / tetrahydrofuran / 8 h / Ambient temperature

With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In tetrahydrofuran;
DOI:10.1021/jo00322a024