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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103Generated: October 28, 2026

Sodium borohydride → HCID 19689353, compound

https://huagongshe.com/reaction/2103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-Chloro-4'-trifluoromethylsulfonylmethylbenzophenoneHCID 11132212—
SolventMethanolHCID 887—
ProductHCID 19689353HCID 1968935377%

Reaction Steps

4-chloro-4'-trifluoromethylsulfonylmethylbenzophenone (5.5 g) was dispersed in methanol (200 ml). Sodium borohydride was gradually added thereto at room temperature with stirring, and the mixture was further stirred overnight at room temperature. After completion of the reaction, methanol was distilled off under reduced pressure. The residue was extracted with ethyl acetate (250 ml). The extract was washed with water and dried over anhydrous magnesium sulfate. Then, ethyl acetate was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=2:1) to obtain the desired product as a white powder (4.2 g, melting point: 113° to 115° C., yield: 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728699
Source datasetuspto-grants-1998_03
ORD IDord-0d7170f4c2ba43dc88cc7ef00696f625
Source noteuspto-grants-1998_03