(S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one

Base Information

Chemical Name:(S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one
CAS No.:211444-56-3
Molecular Formula:C₁₈H₁₈FNO₃
Molecular Weight:315.344
Hs Code.:

Synonyms:(S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one

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Chemical Property of (S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one

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Technology Process of (S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one

There total 1 articles about (S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one 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:

: 90719-32-7
(S)-4-Benzyl-2-oxazolidinone

: 211444-56-3
(S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) MeMgBr / 1.) THF, a) -78 deg C, 10 min, b) 0 deg C, 10 min, 2.) THF, a) -78 deg C, 45 min, b) 0 deg C, 2 h, c) RT, 3 h

2: 1.) Et₂AlCl / 1.) CH₂Cl₂, hexane, -100 deg C, 5 min, 2.) CH₂Cl₂, hexane, -100 deg C, 45 min

With methylmagnesium bromide; diethylaluminium chloride;
DOI:10.1016/S0957-4166(98)00195-5

Reference yield: 98.0%

: 15082-42-5
lithium benzyloxide

: 211444-56-3
(S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one

: 211444-62-1
benzyl (1S,2S,4S)-2-fluorobicyclo[2.2.1]hept-5-ene-2-carboxylate

Guidance literature:: In tetrahydrofuran; at 0 - 20 ℃; for 4h;
DOI:10.1016/S0957-4166(98)00195-5

Reference yield:

: 211444-56-3
(S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one

: 211444-70-1,211444-72-3
(1S,2S,4S)-2-Fluoro-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / tetrahydrofuran / 4 h / 0 - 20 °C

2: 75 percent / 1 N NaOH / tetrahydrofuran / 4 h / Ambient temperature

With sodium hydroxide; In tetrahydrofuran;
DOI:10.1016/S0957-4166(98)00195-5