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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767195Generated: November 3, 2026

Benzyl Bromide → HCID 10195119, compound

https://huagongshe.com/reaction/1767195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 21112938HCID 21112938—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 10195119HCID 10195119—

Reaction Steps

3-{2-[5-Bromo-2-(hydroxy)-phenyl]-cyclopent-1-enyl}-benzoic acid (0.04 g, 0.12 mmol), benzyl bromide (0.038 g, 0.22 moles), potassium hydroxide (˜0.15 g), in dimethyl sulphoxide (1.5 mL) were stirred at room temperature over 8 hrs under nitrogen. The reaction mixture was then quenched with ice/water (10/10 mL), stirred at room temperature for ˜1.5 hrs, acidified with 2N hydrochloric acid to pH˜3 and extracted with dichloromethane. The organic extract was then dried (magnesium sulphate) and concentrated down to an oil and was then chromatographed on Waters sep-pak cartridge (10 g) giving (0.028 g, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232821B2
Source datasetuspto-grants-2007_06
ORD IDord-f237dc07b6c74dfebebeadfbdc48ceed
Source noteuspto-grants-2007_06