2-benzylsulfonyloxirane

Base Information

Chemical Name:2-benzylsulfonyloxirane
CAS No.:190841-30-6
Molecular Formula:C₉H₁₀O₃S
Molecular Weight:198.243
Hs Code.:

Synonyms:2-benzylsulfonyloxirane

Suppliers and Price of 2-benzylsulfonyloxirane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-benzylsulfonyloxirane

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-benzylsulfonyloxirane

There total 5 articles about 2-benzylsulfonyloxirane 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: 71.0%

: 15753-89-6
((vinylsulfonyl)methyl)benzene

: 190841-30-6
2-benzylsulfonyloxirane

Guidance literature:: With lithium tert-butyl hydroperoxide; at -78 - 0 ℃;
DOI:10.1016/S0040-4039(97)00507-8

Reference yield:

: 3878-41-9
2-(benzylthio)ethanol

: 190841-30-6
2-benzylsulfonyloxirane

Guidance literature:: Multi-step reaction with 3 steps

1: NaBO₃*4H₂O / acetic acid / 20 °C

2: methanesulfonyl chloride; triethylamine / CH₂Cl₂ / 20 °C

3: LiO₂tBu / tetrahydrofuran

With sodium perborate; lithium tert-butyl hydroperoxide; methanesulfonyl chloride; triethylamine; In tetrahydrofuran; dichloromethane; acetic acid; 3: Meth-Cohn epoxidation;
DOI:10.1002/ejoc.200500956

Reference yield:

: 16793-42-3
benzyl 2-hydroxyethyl sulfone

: 190841-30-6
2-benzylsulfonyloxirane

Guidance literature:: Multi-step reaction with 2 steps

1: methanesulfonyl chloride; triethylamine / CH₂Cl₂ / 20 °C

2: LiO₂tBu / tetrahydrofuran

With lithium tert-butyl hydroperoxide; methanesulfonyl chloride; triethylamine; In tetrahydrofuran; dichloromethane; 2: Meth-Cohn epoxidation;
DOI:10.1002/ejoc.200500956