tert-butyl 4(R)-<(1'S,2'R,3'S)-2'-(ethoxycarbonyl)-3'-phenylcyclopropyl>-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

Base Information

Chemical Name:tert-butyl 4(R)-<(1'S,2'R,3'S)-2'-(ethoxycarbonyl)-3'-phenylcyclopropyl>-2,2-dimethyl-1,3-oxazolidine-3-carboxylate
CAS No.:236751-33-0
Molecular Formula:C₂₂H₃₁NO₅
Molecular Weight:389.492
Hs Code.:

Synonyms:tert-butyl 4(R)-<(1'S,2'R,3'S)-2'-(ethoxycarbonyl)-3'-phenylcyclopropyl>-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

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Chemical Property of tert-butyl 4(R)-<(1'S,2'R,3'S)-2'-(ethoxycarbonyl)-3'-phenylcyclopropyl>-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

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Technology Process of tert-butyl 4(R)-<(1'S,2'R,3'S)-2'-(ethoxycarbonyl)-3'-phenylcyclopropyl>-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

There total 3 articles about tert-butyl 4(R)-<(1'S,2'R,3'S)-2'-(ethoxycarbonyl)-3'-phenylcyclopropyl>-2,2-dimethyl-1,3-oxazolidine-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: 26.0%

: 623-73-4
diazoacetic acid ethyl ester

: 132652-65-4
tert-butyl 2,2-dimethyl-4-[(E)-2-phenylethenyl]-1,3-oxazolane-3-carboxylate

: 236751-33-0
tert-butyl 4(R)-<(1'S,2'R,3'S)-2'-(ethoxycarbonyl)-3'-phenylcyclopropyl>-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

Guidance literature:: With dirhodium tetraacetate; In dichloromethane;
DOI:10.1021/jm990128v

Reference yield:

: 102308-32-7
(4S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

: 236751-33-0
tert-butyl 4(R)-<(1'S,2'R,3'S)-2'-(ethoxycarbonyl)-3'-phenylcyclopropyl>-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-BuLi / 1.) hexane, 30 min, 2.) hexane, overnight

2: 26 percent / Rh₂(OAc)4 / CH₂Cl₂

With dirhodium tetraacetate; n-butyllithium; In dichloromethane;
DOI:10.1021/jm990128v

Reference yield:

: 1449-46-3
benzyltriphenylphosphonium bromide

: 236751-33-0
tert-butyl 4(R)-<(1'S,2'R,3'S)-2'-(ethoxycarbonyl)-3'-phenylcyclopropyl>-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-BuLi / 1.) hexane, 30 min, 2.) hexane, overnight

2: 26 percent / Rh₂(OAc)4 / CH₂Cl₂

With dirhodium tetraacetate; n-butyllithium; In dichloromethane;
DOI:10.1021/jm990128v