(R)-benzyl 4-((R)-hydroxy(4-methoxyphenyl)methyl)-2,2-dimethyloxazolidine-3-carboxylate

Base Information

Chemical Name:(R)-benzyl 4-((R)-hydroxy(4-methoxyphenyl)methyl)-2,2-dimethyloxazolidine-3-carboxylate
CAS No.:1092473-67-0
Molecular Formula:C₂₁H₂₅NO₅
Molecular Weight:371.433
Hs Code.:

Synonyms:(R)-benzyl 4-((R)-hydroxy(4-methoxyphenyl)methyl)-2,2-dimethyloxazolidine-3-carboxylate

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Chemical Property of (R)-benzyl 4-((R)-hydroxy(4-methoxyphenyl)methyl)-2,2-dimethyloxazolidine-3-carboxylate

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Technology Process of (R)-benzyl 4-((R)-hydroxy(4-methoxyphenyl)methyl)-2,2-dimethyloxazolidine-3-carboxylate

There total 4 articles about (R)-benzyl 4-((R)-hydroxy(4-methoxyphenyl)methyl)-2,2-dimethyloxazolidine-3-carboxylate 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: 92.0%

: 104-92-7
1-bromo-4-methoxy-benzene

: 133464-37-6
(4R)-4-formyl-2,2-dimethyloxazolidine-3-carboxylic acid benzyl ester

: 1092473-67-0
(R)-benzyl 4-((R)-hydroxy(4-methoxyphenyl)methyl)-2,2-dimethyloxazolidine-3-carboxylate

Guidance literature:: 1-bromo-4-methoxy-benzene; With magnesium; ethylene dibromide; In tetrahydrofuran; at 65 ℃; Reflux;

With copper(l) iodide; dimethylsulfide; In tetrahydrofuran; at -78 - 20 ℃;

(4R)-4-formyl-2,2-dimethyloxazolidine-3-carboxylic acid benzyl ester; In tetrahydrofuran; at -78 - 10 ℃;

Reference yield:

: 6081-61-4
N-(benzyloxycarbonyl)-D-serine

: 1092473-67-0
(R)-benzyl 4-((R)-hydroxy(4-methoxyphenyl)methyl)-2,2-dimethyloxazolidine-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride

2.1: boron trifluoride diethyl etherate; triethylamine / acetone / 5 h / 20 °C

3.1: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / -15 °C

4.1: magnesium / tetrahydrofuran; ethylenediamine / 2 h / Reflux

4.2: 0.5 h / -78 - -45 °C

With lithium aluminium tetrahydride; boron trifluoride diethyl etherate; magnesium; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; ethylenediamine; acetone;

Reference yield:

: 656827-13-3
(R)-benzyl-4-(methoxy(methyl)carbamoyl)-2,2-dimethyloxazolidine-3-carboxylate

: 1092473-67-0
(R)-benzyl 4-((R)-hydroxy(4-methoxyphenyl)methyl)-2,2-dimethyloxazolidine-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / -15 °C

2.1: magnesium / tetrahydrofuran; ethylenediamine / 2 h / Reflux

2.2: 0.5 h / -78 - -45 °C

With lithium aluminium tetrahydride; magnesium; In tetrahydrofuran; ethylenediamine;