3-Benzenesulfinyl-7-oxo-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid benzhydryl ester

Base Information

Chemical Name:3-Benzenesulfinyl-7-oxo-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid benzhydryl ester
CAS No.:102045-97-6
Molecular Formula:C₂₇H₂₂O₄S
Molecular Weight:442.535
Hs Code.:

Synonyms:3-Benzenesulfinyl-7-oxo-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid benzhydryl ester

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Chemical Property of 3-Benzenesulfinyl-7-oxo-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid benzhydryl ester

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Technology Process of 3-Benzenesulfinyl-7-oxo-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid benzhydryl ester

There total 9 articles about 3-Benzenesulfinyl-7-oxo-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid benzhydryl 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: 79.0%

: 97517-30-1
3-phenylthio-7-oxobicyclo[3.2.0]hept-2-en-2-carboxylic acid, diphenyl methyl ester

: 102045-97-6
3-Benzenesulfinyl-7-oxo-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid benzhydryl ester

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at -40 ℃; for 1h;
DOI:10.1016/S0040-4039(00)98208-X

Reference yield:

: 97517-25-4
silyloxyfulvene

: 102045-97-6
3-Benzenesulfinyl-7-oxo-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid benzhydryl ester

Guidance literature:: Multi-step reaction with 8 steps

1: Et₃N / cyclohexane / 1.5 h / Ambient temperature

2: 34 percent / 50 percent HF / acetonitrile / 0.58 h / Heating

3: Jones reagent / acetone / 0.75 h / 20 °C

4: ethyl acetate / 1 h / Ambient temperature

5: Zn / tetrahydrofuran; acetic acid / 6 h / Ambient temperature

6: Et₃N / tetrahydrofuran / 1 h / Ambient temperature

7: SO₂Cl₂, pyridine / CH₂Cl₂ / 0.5 h / -60 °C

8: 79 percent / MCPBA / CH₂Cl₂ / 1 h / -40 °C

With pyridine; sulfuryl dichloride; jones reagent; hydrogen fluoride; triethylamine; 3-chloro-benzenecarboperoxoic acid; zinc; In tetrahydrofuran; dichloromethane; cyclohexane; acetic acid; ethyl acetate; acetone; acetonitrile;
DOI:10.1016/S0040-4039(00)98208-X

Reference yield:

: 97517-24-3
6,6-Dichloro-7-oxobicyclo[3.2.0]hept-2-en-2-carboxaldehyde

: 102045-97-6
3-Benzenesulfinyl-7-oxo-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid benzhydryl ester

Guidance literature:: Multi-step reaction with 6 steps

1: Jones reagent / acetone / 0.75 h / 20 °C

2: ethyl acetate / 1 h / Ambient temperature

3: Zn / tetrahydrofuran; acetic acid / 6 h / Ambient temperature

4: Et₃N / tetrahydrofuran / 1 h / Ambient temperature

5: SO₂Cl₂, pyridine / CH₂Cl₂ / 0.5 h / -60 °C

6: 79 percent / MCPBA / CH₂Cl₂ / 1 h / -40 °C

With pyridine; sulfuryl dichloride; jones reagent; triethylamine; 3-chloro-benzenecarboperoxoic acid; zinc; In tetrahydrofuran; dichloromethane; acetic acid; ethyl acetate; acetone;
DOI:10.1016/S0040-4039(00)98208-X