Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802440Generated: November 2, 2026

tert-Butyldiphenylchlorosilane → HCID 59268006, compound

https://huagongshe.com/reaction/1802440

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
ReactantHCID 59267935HCID 59267935—
SolventDichloromethaneHCID 6344—
ProductHCID 59268006HCID 59268006116.1%

Reaction Steps

To a solution of 0.41 g (0.96 mmol) of N-[3-(2-hydroxy-1,1-dimethyl-ethyl)-isoxazol-5-yl]-2-(4-methoxy-cyclohexylmethanesulfonyl)-2-methyl-propionamide in DCM (8 ml) are added imidazoles (0.07 g, 0.96 mmol), followed by tert-Butylchlorodiphenylsilane (0.26 g, 0.96 mmol). The reaction is stirred at room temperature for 20 h. The mixture is diluted with DCM (10 mL) and washed with saturated aqueous NH4Cl solution, brine, dried (MgSO4) and filtered. The filtrate is concentrated under reduced pressure to give 0.73 g of N-{3-[2-(tert-butyl-diphenyl-silanyloxy)-1,1-dimethyl-ethyl]-isoxazol-5-yl}-2-(4-methoxy-cyclohexylmethanesulfonyl)-2-methyl-propionamide. Yield: 100%, ES-MS: 655 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349871B2
Source datasetuspto-grants-2013_01
ORD IDord-bb2e665224cf459b935317240118ec0a
Source noteuspto-grants-2013_01