(3R,4S,5R)-ethyl 2-benzyl-4-formyl-3,5-dimethylisoxazolidine-3-carboxylate

Base Information

Chemical Name:(3R,4S,5R)-ethyl 2-benzyl-4-formyl-3,5-dimethylisoxazolidine-3-carboxylate
CAS No.:1373354-07-4
Molecular Formula:C₁₆H₂₁NO₄
Molecular Weight:291.347
Hs Code.:

Synonyms:(3R,4S,5R)-ethyl 2-benzyl-4-formyl-3,5-dimethylisoxazolidine-3-carboxylate

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Chemical Property of (3R,4S,5R)-ethyl 2-benzyl-4-formyl-3,5-dimethylisoxazolidine-3-carboxylate

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Technology Process of (3R,4S,5R)-ethyl 2-benzyl-4-formyl-3,5-dimethylisoxazolidine-3-carboxylate

There total 8 articles about (3R,4S,5R)-ethyl 2-benzyl-4-formyl-3,5-dimethylisoxazolidine-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: 75.0%

: 123-73-9,4170-30-3
trans-Crotonaldehyde

: 1373353-97-9
(E)-N-(1-ethoxy-1-oxopropan-2-ylidene)(phenyl)methanamine N-oxide

: 1373354-07-4
(3R,4S,5R)-ethyl 2-benzyl-4-formyl-3,5-dimethylisoxazolidine-3-carboxylate

Guidance literature:: (E)-N-(1-ethoxy-1-oxopropan-2-ylidene)(phenyl)methanamine N-oxide; With (5S)-(?)-2,2,3-trimethyl-5-benzyl-4-imidazolidinone monohydrochloride; In nitromethane; at -10 ℃; for 0.166667h; Inert atmosphere;

trans-Crotonaldehyde; In nitromethane; for 120h; enantioselective reaction; Inert atmosphere;
DOI:10.1016/j.tetasy.2012.11.010

Reference yield:

: 123-73-9,4170-30-3
trans-Crotonaldehyde

: 1373353-97-9
(E)-N-(1-ethoxy-1-oxopropan-2-ylidene)(phenyl)methanamine N-oxide

: 1373354-25-6
(3R,4S,5R)-ethyl 2-benzyl-4-formyl-3,5-dimethylisoxazolidine-3-carboxylate

: 1373354-07-4
(3R,4S,5R)-ethyl 2-benzyl-4-formyl-3,5-dimethylisoxazolidine-3-carboxylate

Guidance literature:: With (5R)-(+)-2,2,3-trimethyl-5-benzyl-4-imidazolidinone monohydrochloride; water; In nitromethane; at 20 ℃; for 22h; optical yield given as %ee; enantioselective reaction;
DOI:10.1016/j.tetasy.2012.02.003

Reference yield:

: 617-35-6
2-oxo-propionic acid ethyl ester

: 1373354-07-4
(3R,4S,5R)-ethyl 2-benzyl-4-formyl-3,5-dimethylisoxazolidine-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

2: (5R)-(+)-2,2,3-trimethyl-5-benzyl-4-imidazolidinone monohydrochloride; water / nitromethane / 22 h / 20 °C

With (5R)-(+)-2,2,3-trimethyl-5-benzyl-4-imidazolidinone monohydrochloride; water; In nitromethane;
DOI:10.1016/j.tetasy.2012.02.003