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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636727Generated: October 30, 2026

Hexamethyldisilazane → HCID 18434188, compound

https://huagongshe.com/reaction/1636727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethyldisilazaneHCID 13838—
Reactant(4-Bromophenyl)(4-hydroxyphenyl)methanoneHCID 4570728—
ProductHCID 18434188HCID 18434188—

Reaction Steps

Ea) A mixture of 2.77 g of 4-hydroxyphenyl-(4-bromo-phenyl)-methanone and 50 ml of hexamethyidisilazane is heated under reflux for 4 h., then concentrated and dried. The resulting 4-trimethylsilyloxyphenyl-(4-bromo-phenyl)-methanone is dissolved in 60 ml of toluene and treated at room temperature under argon with 11 ml of methylmagnesium chloride solution (22% in THF). The mixture is boiled under reflux. After cooling the mixture is treated with saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic phases are washed with saturated sodium chloride solution and dried. After evaporation of the ethyl acetate extracts there are obtained 3.36 g of (RS)-4-[1-(4-bromo-phenyl)-1-hydroxy-ethyl]-phenol, MS: m/e 293 (M+H+, 1Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034275
Source datasetuspto-grants-2000_03
ORD IDord-3fad31b2ff08490cb968a104322d4314
Source noteuspto-grants-2000_03