(4R,5R)-3-Benzyl-5-isopropyl-2-oxo-oxazolidine-4-carboxylic acid methyl ester

Base Information

Chemical Name:(4R,5R)-3-Benzyl-5-isopropyl-2-oxo-oxazolidine-4-carboxylic acid methyl ester
CAS No.:176541-58-5
Molecular Formula:C₁₅H₁₉NO₄
Molecular Weight:277.32
Hs Code.:

Synonyms:(4R,5R)-3-Benzyl-5-isopropyl-2-oxo-oxazolidine-4-carboxylic acid methyl ester

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Chemical Property of (4R,5R)-3-Benzyl-5-isopropyl-2-oxo-oxazolidine-4-carboxylic acid methyl ester

Chemical Property:

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Technology Process of (4R,5R)-3-Benzyl-5-isopropyl-2-oxo-oxazolidine-4-carboxylic acid methyl ester

There total 6 articles about (4R,5R)-3-Benzyl-5-isopropyl-2-oxo-oxazolidine-4-carboxylic 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:

Reference yield:

: 97906-31-5
(2R,3R)-(3-isopropyloxiran-2-yl)methanol

: 176541-58-5
(4R,5R)-3-Benzyl-5-isopropyl-2-oxo-oxazolidine-4-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: NaH / tetrahydrofuran / 3 h / Heating

2: CrO₃, H₂SO₄ / acetone; H₂O / 1 h / Ambient temperature

3: diethyl ether

With chromium(VI) oxide; sulfuric acid; sodium hydride; In tetrahydrofuran; diethyl ether; water; acetone;
DOI:10.1021/ja9541544

Reference yield:

: 176541-56-3
(4S,5R)-3-Benzyl-4-hydroxymethyl-5-isopropyl-oxazolidin-2-one

: 176541-58-5
(4R,5R)-3-Benzyl-5-isopropyl-2-oxo-oxazolidine-4-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: CrO₃, H₂SO₄ / acetone; H₂O / 1 h / Ambient temperature

2: diethyl ether

With chromium(VI) oxide; sulfuric acid; In diethyl ether; water; acetone;
DOI:10.1021/ja9541544

Reference yield:

: 3173-56-6
benzyl isothiocyanate

: 176541-58-5
(4R,5R)-3-Benzyl-5-isopropyl-2-oxo-oxazolidine-4-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: NaH / tetrahydrofuran / 3 h / Heating

2: CrO₃, H₂SO₄ / acetone; H₂O / 1 h / Ambient temperature

3: diethyl ether

With chromium(VI) oxide; sulfuric acid; sodium hydride; In tetrahydrofuran; diethyl ether; water; acetone;
DOI:10.1021/ja9541544