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(2R,3S)-2-benzyl-3,4-(benzyloxycarbonylimino)-butanoic acid methyl ester

Base Information Edit
  • Chemical Name:(2R,3S)-2-benzyl-3,4-(benzyloxycarbonylimino)-butanoic acid methyl ester
  • CAS No.:349148-42-1
  • Molecular Formula:C20H21NO4
  • Molecular Weight:339.391
  • Hs Code.:
  • Mol file:349148-42-1.mol
(2R,3S)-2-benzyl-3,4-(benzyloxycarbonylimino)-butanoic acid methyl ester

Synonyms:(2R,3S)-2-benzyl-3,4-(benzyloxycarbonylimino)-butanoic acid methyl ester

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Chemical Property of (2R,3S)-2-benzyl-3,4-(benzyloxycarbonylimino)-butanoic acid methyl ester Edit
Chemical Property:
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Technology Process of (2R,3S)-2-benzyl-3,4-(benzyloxycarbonylimino)-butanoic acid methyl ester

There total 7 articles about (2R,3S)-2-benzyl-3,4-(benzyloxycarbonylimino)-butanoic acid methyl 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:
Guidance literature:
With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 0 ℃; for 3h;
DOI:10.1021/jo0014055
Guidance literature:
Multi-step reaction with 6 steps
1.1: LiHMDS / tetrahydrofuran; hexane / 2 h / -78 °C
1.2: 56 percent / tetrahydrofuran; hexane / 6 h
2.1: acetyl chloride / methanol / 3 h / 0 °C
2.2: CuCO3*Cu(OH)2 / H2O / 3 h / 70 °C
3.1: 5.8 g / Na2CO3 / H2O / 4 h / 20 °C
4.1: DCC / 1,2-dimethoxy-ethane
5.1: 7.3 g / NaBH4 / tetrahydrofuran / 18 h / 0 - 20 °C
6.1: 82 percent / DEAD; PPh3 / tetrahydrofuran / 3 h / 0 °C
With sodium tetrahydroborate; sodium carbonate; acetyl chloride; dicyclohexyl-carbodiimide; triphenylphosphine; lithium hexamethyldisilazane; diethylazodicarboxylate; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; hexane; water; 6.1: Intramolecular Mitsunobu reaction;
DOI:10.1021/jo0014055
Guidance literature:
Multi-step reaction with 6 steps
1.1: LiHMDS / tetrahydrofuran; hexane / 2 h / -78 °C
1.2: 56 percent / tetrahydrofuran; hexane / 6 h
2.1: acetyl chloride / methanol / 3 h / 0 °C
2.2: CuCO3*Cu(OH)2 / H2O / 3 h / 70 °C
3.1: 5.8 g / Na2CO3 / H2O / 4 h / 20 °C
4.1: DCC / 1,2-dimethoxy-ethane
5.1: 7.3 g / NaBH4 / tetrahydrofuran / 18 h / 0 - 20 °C
6.1: 82 percent / DEAD; PPh3 / tetrahydrofuran / 3 h / 0 °C
With sodium tetrahydroborate; sodium carbonate; acetyl chloride; dicyclohexyl-carbodiimide; triphenylphosphine; lithium hexamethyldisilazane; diethylazodicarboxylate; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; hexane; water; 6.1: Intramolecular Mitsunobu reaction;
DOI:10.1021/jo0014055
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