6-benzyloxy-3-(2-oxo-oxazolidine-3-carbonyl)-hexanoic acid trityloxy-amide

Base Information

Chemical Name:6-benzyloxy-3-(2-oxo-oxazolidine-3-carbonyl)-hexanoic acid trityloxy-amide
CAS No.:928617-94-1
Molecular Formula:C₃₆H₃₆N₂O₆
Molecular Weight:592.692
Hs Code.:

Synonyms:6-benzyloxy-3-(2-oxo-oxazolidine-3-carbonyl)-hexanoic acid trityloxy-amide

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Chemical Property of 6-benzyloxy-3-(2-oxo-oxazolidine-3-carbonyl)-hexanoic acid trityloxy-amide

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Technology Process of 6-benzyloxy-3-(2-oxo-oxazolidine-3-carbonyl)-hexanoic acid trityloxy-amide

There total 7 articles about 6-benzyloxy-3-(2-oxo-oxazolidine-3-carbonyl)-hexanoic acid trityloxy-amide 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: 80.0%

: 913987-02-7
6-(benzyloxy)-3-(2-oxooxazolidine-3-carbonyl)hexanoic acid

: 31938-11-1
O-tritylhydroxylamine

: 928617-94-1
6-benzyloxy-3-(2-oxo-oxazolidine-3-carbonyl)-hexanoic acid trityloxy-amide

Guidance literature:: With dicyclohexyl-carbodiimide; In dichloromethane;
DOI:10.1039/b609446e

Reference yield:

: 913987-01-6
3-(5-(benzyloxy)pentanoyl)oxazolidin-2-one

: 928617-94-1
6-benzyloxy-3-(2-oxo-oxazolidine-3-carbonyl)-hexanoic acid trityloxy-amide

Guidance literature:: Multi-step reaction with 3 steps

1: 71 percent / NaHMDS

2: 99 percent / TFA / CH₂Cl₂

3: 80 percent / DCC / CH₂Cl₂

With sodium hexamethyldisilazane; dicyclohexyl-carbodiimide; trifluoroacetic acid; In dichloromethane;
DOI:10.1039/b609446e

Reference yield:

: 928617-86-1
6-benzyloxy-3-(2-oxo-oxazolidine-3-carbonyl)-hexanoic acid tert-butyl ester

: 928617-94-1
6-benzyloxy-3-(2-oxo-oxazolidine-3-carbonyl)-hexanoic acid trityloxy-amide

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / TFA / CH₂Cl₂

2: 80 percent / DCC / CH₂Cl₂

With dicyclohexyl-carbodiimide; trifluoroacetic acid; In dichloromethane;
DOI:10.1039/b609446e