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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859537Generated: October 26, 2026

Acetone → 2-(3,5-Dibromothiophen-2-yl)propan-2-ol

https://huagongshe.com/reaction/1859537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHexaneHCID 8058—
ReactantThiophene, 2,3,5-tribromo-HCID 76592—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product2-(3,5-Dibromothiophen-2-yl)propan-2-olHCID 22572727—

Reaction Steps

A solution of 2,3,5-tribromothiophene (8.17 g, 25 mmol) in Et2O (N2 atmosphere) was cooled to −78° C. and treated with a 1.6 M hexane solution of nBuLi (15.6 mL, 25 mmol). The mixture was then stirred for 10 minutes, then treated with acetone (1.84 mL, 25 mmol). The mixture was then stirred for 30 minutes and quenched with H2O. The mixture was extracted with Et2O; the organic layers were combined, dried (MgSO4), and the solvent removed in vacuo. The residue was filtered through a plug of silica gel (gradient elution from hexanes to EtOAc) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528510B1
Source datasetuspto-grants-2003_03
ORD IDord-9efd2e7c19d04d248fc0530be543a158
Source noteuspto-grants-2003_03