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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384256Generated: October 27, 2026

Potassium Hydroxide → 1-Bromo-4-(cyclopropylmethyl)benzene

https://huagongshe.com/reaction/1384256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant4-Bromophenyl cyclopropyl ketoneHCID 81394—
SolventEthylene GlycolHCID 174—
Product1-Bromo-4-(cyclopropylmethyl)benzeneHCID 1165139749.2%

Reaction Steps

4-Bromophenyl cyclopropyl ketone (5.63 g), hydrazine monohydrate (2.5 ml) and potassium hydroxide (3.33 g) were added to ethylene glycol (25 ml) and the mixture heated to reflux for 1 hour. The reaction mixture was cooled and partitioned between water (20 ml) and ethyl acetate (30 ml) and the organic layer was separated. The aqueous layer was extracted with ethyl acetate (30 ml) and the combined organic phases were washed with 2M hydrochloric acid (15 ml) and water (15 ml) then dried (MgSO4) and evaporated. The residue was purified by chromatography on a Mega Bond Elut column, eluting with hexane to give 1-bromo-4-(cyclopropylmethyl)benzene (2.6 g); 1H NMR (CDCl3): 0.2 (m, 2H), 0.55 (m, 2H), 2.50 (d, 2H), 7.14 (d, 2H), 7.41 (d, 2H); mass spectrum (EI+) 210 (M.)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258817B1
Source datasetuspto-grants-2001_07
ORD IDord-b0dc0e857a85423a8741b4e64ca2367c
Source noteuspto-grants-2001_07