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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196544Generated: October 30, 2026

Sodium borohydride → HCID 54231897, compound

https://huagongshe.com/reaction/1196544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13948318HCID 13948318—
SolventEthanolHCID 702—
ProductHCID 54231897HCID 54231897—

Reaction Steps

4-[N-Benzylmethanesulphonamido]phenacyl bromide (30 g) and sodium borohydride (4 g) in ethanol (500 ml) were stirred at room temperature for 18 hours. The solvent was then removed and the residue was taken up in ethyl acetate and washed three times with sodium bicarbonate solution and three times with brine. The organic phase was dried and evaporated to give an oil which was chromatographed on silica, "Kieselgel 60" (Merck, Trade Mark), eluting with methylene chloride. The product-containing fractions were combined and evaporated to give a solid which was triturated with hexane and filtered off to give the title compound, yield 13 g, m.p. 89°-92°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05114952
Source datasetuspto-grants-1992_05
ORD IDord-8ed130a5930942b195ab0a67c75a4016
Source noteuspto-grants-1992_05