S-α-phenylsulfonylmethylbenzyl alcohol

Base Information

Chemical Name:S-α-phenylsulfonylmethylbenzyl alcohol
CAS No.:224634-51-9
Molecular Formula:C₁₄H₁₄O₃S
Molecular Weight:262.329
Hs Code.:

Synonyms:S-α-phenylsulfonylmethylbenzyl alcohol

Suppliers and Price of S-α-phenylsulfonylmethylbenzyl alcohol

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

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Chemical Property of S-α-phenylsulfonylmethylbenzyl alcohol

Chemical Property:

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Technology Process of S-α-phenylsulfonylmethylbenzyl alcohol

There total 19 articles about S-α-phenylsulfonylmethylbenzyl alcohol 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: 99.0%

: 3406-03-9
2-(phenylsulfonyl)acetophenone

: 224634-51-9
S-α-phenylsulfonylmethylbenzyl alcohol

Guidance literature:: With sodium tetrahydroborate; chloro-trimethyl-silane; polymer-supported chiral sulfonamide; In tetrahydrofuran; Heating;
DOI:10.1016/S0957-4166(02)00546-3

Reference yield: 95.0%

: 873-55-2
sodium benzenesulfonate

: 70-11-1
α-bromoacetophenone

: 224634-51-9
S-α-phenylsulfonylmethylbenzyl alcohol

Guidance literature:: With chloro([(S,2S)-(?)-2-amino-1,2-diphenylethyl](4-toluenesulfonyl)amido)(mesitylene)ruthenium (II); sodium formate; In methanol; water; at 50 ℃; for 1h; Solvent; Temperature; enantioselective reaction;
DOI:10.1021/ol502832a

Reference yield: 91.0%

: 873-55-2
sodium benzenesulfonate

: 536-74-3
phenylacetylene

: 224634-51-9
S-α-phenylsulfonylmethylbenzyl alcohol

Guidance literature:: sodium benzenesulfonate; phenylacetylene; In ethanol; water; at 50 ℃;

With sodium formate; In ethanol; water; at 50 ℃; Reagent/catalyst; enantioselective reaction;
DOI:10.1002/cctc.202001553