Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65266Generated: October 29, 2026

Benzyl Bromide → HCID 13518986, compound

https://huagongshe.com/reaction/65266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium HydroxideHCID 14797—
Reactantalpha-Mercaptomethyl-beta-(p-nitrophenyl)-gamma-butyrolactoneHCID 20234198—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 13518986HCID 1351898663.6%

Reaction Steps

To a solution of 71 mg of potassium hydroxide in 6 ml of ethanol were added 253 mg of α-mercaptomethyl-β-(p-nitrophenyl)-γ-butyrolactone and 239 mg of benzyl bromide and the resulting mixture was kept at room temperature for 4 hours. After completion of the reaction, the reaction mixture was diluted with 60 ml of ethyl acetate, washed with water and saturated saline, dried over magnesium sulfate and the solvent was distilled off. The resulting crude product was purified by a silica gel column chromatography to give 218 mg (yield 50%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04613613
Source datasetuspto-grants-1986_09
ORD IDord-2cafb935f8da4155af7d1e7301adc72b
Source noteuspto-grants-1986_09