(S)-3-(3-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

Base Information

Chemical Name:(S)-3-(3-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide
CAS No.:1166859-74-0
Molecular Formula:C₂₀H₂₇NO₃SSi
Molecular Weight:389.591
Hs Code.:

Synonyms:(S)-3-(3-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

Suppliers and Price of (S)-3-(3-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

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 (S)-3-(3-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-3-(3-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

There total 5 articles about (S)-3-(3-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide 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%

: 1166859-56-8
3-[(t-butyldimethylsilyloxy)methyl]-phenyl-1,2-benzothiazole 1,1-dioxide

: 1166859-74-0
(S)-3-(3-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

Guidance literature:: With C₄₀H₄₄IrN₆⁽¹⁺⁾*F₆P^(1-); ammonium formate; In water; N,N-dimethyl-formamide; at 60 ℃; for 4h; enantioselective reaction;
DOI:10.1039/c7cc04691j

Reference yield: 91.0%

: 1609692-27-4
(S,S_S)-3-[(tert-butyldimethylsilyloxy)methyl]phenyl-2,3-dihydrobenzo[d]isothiazole-1-oxide

: 1166859-74-0
(S)-3-(3-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 ℃; for 0.5h;
DOI:10.1039/c4cc01831a

Reference yield:

: 1609692-17-2
(S,R_S)-N-[(2-bromophenyl)(3-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)methyl]-2-methylpropane-2-sulfinamide

: 1166859-74-0
(S)-3-(3-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide

Guidance literature:: Multi-step reaction with 2 steps

1: tri-n-butyl-tin hydride; 2,2'-azobis(isobutyronitrile) / toluene / 6 h / 110 °C

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0.5 h / 0 °C

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; toluene;
DOI:10.1039/c4cc01831a