(4R,5S)-5-(3-Benzyloxy-propyl)-4-methyl-oxazolidine-3-carboxylic acid cyclohexyl ester

Base Information

Chemical Name:(4R,5S)-5-(3-Benzyloxy-propyl)-4-methyl-oxazolidine-3-carboxylic acid cyclohexyl ester
CAS No.:126260-83-1
Molecular Formula:C₂₁H₃₁NO₄
Molecular Weight:361.481
Hs Code.:

Synonyms:(4R,5S)-5-(3-Benzyloxy-propyl)-4-methyl-oxazolidine-3-carboxylic acid cyclohexyl ester

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Chemical Property of (4R,5S)-5-(3-Benzyloxy-propyl)-4-methyl-oxazolidine-3-carboxylic acid cyclohexyl ester

Chemical Property:

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Technology Process of (4R,5S)-5-(3-Benzyloxy-propyl)-4-methyl-oxazolidine-3-carboxylic acid cyclohexyl ester

There total 14 articles about (4R,5S)-5-(3-Benzyloxy-propyl)-4-methyl-oxazolidine-3-carboxylic acid cyclohexyl 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:

: 5470-84-8
4-benzyloxybutanal

: 126260-83-1
(4R,5S)-5-(3-Benzyloxy-propyl)-4-methyl-oxazolidine-3-carboxylic acid cyclohexyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 66 percent / tetrahydrofuran

2: 53 percent / p-TsOH / diethyl ether / 0.67 h / Heating

3: 1.) Hg(OAc)2, 2.) NaBH₄, KOH / 1.) CH₃CN, 2.) CH₂Cl₂

With potassium hydroxide; sodium tetrahydroborate; mercury(II) diacetate; toluene-4-sulfonic acid; In tetrahydrofuran; diethyl ether;

Reference yield:

: 5470-84-8
4-benzyloxybutanal

: 126260-83-1
(4R,5R)-5-(3-Benzyloxy-propyl)-4-methyl-oxazolidine-3-carboxylic acid cyclohexyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 66 percent / tetrahydrofuran

2: 53 percent / p-TsOH / diethyl ether / 0.67 h / Heating

3: 1.) Hg(OAc)2, 2.) NaBH₄, KOH / 1.) CH₃CN, 2.) CH₂Cl₂

With potassium hydroxide; sodium tetrahydroborate; mercury(II) diacetate; toluene-4-sulfonic acid; In tetrahydrofuran; diethyl ether;

Reference yield:

: 4541-14-4
4-benzyloxy-butan-1-ol

: 126260-83-1
(4R,5S)-5-(3-Benzyloxy-propyl)-4-methyl-oxazolidine-3-carboxylic acid cyclohexyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / PCC / CH₂Cl₂

2: 66 percent / tetrahydrofuran

3: 53 percent / p-TsOH / diethyl ether / 0.67 h / Heating

4: 1.) Hg(OAc)2, 2.) NaBH₄, KOH / 1.) CH₃CN, 2.) CH₂Cl₂

With potassium hydroxide; sodium tetrahydroborate; mercury(II) diacetate; toluene-4-sulfonic acid; pyridinium chlorochromate; In tetrahydrofuran; diethyl ether; dichloromethane;