Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30562Generated: October 31, 2026

Potassium Hydroxide → Benzene, 1-bromo-3-(4,4,4-trifluorobutyl)-

https://huagongshe.com/reaction/30562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant1-Butanone, 1-(3-bromophenyl)-4,4,4-trifluoro-HCID 57435866—
SolventDiglymeHCID 8150—
ProductBenzene, 1-bromo-3-(4,4,4-trifluorobutyl)-HCID 5743586888%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-(3-bromo-phenyl)-4,4,4-trifluoro-butan-1-one (3.1 g, 11 mmol) and diglyme was treated with hydrazine mono hydrate (5.5 g, 110.3 mmol), and stirred at 100° C. for 2 hours then treated with powder KOH (3.1 g, 55.1 mmol). The stirring continued at 150° C. for 6 hours. The mixture was cooled to room temperature, poured into a mixture of ice/water and extracted with ethyl ether. The extracts were combined, dried over MgSO4 and concentrated in vacuo. The crude product was purified on silica gel (ISCO) using hexanes as the eluting solvent to give 1-Bromo-3-(4,4,4-trifluoro-butyl)-benzene as a colorless oil (2.4 g, 88% yield). m/e (M)+ 266; 1H NMR (400 MHZ, DMSO-d6) δ ppm, 1.7-1.8 (m, 2 H), 2.1-2.2 (m, 2 H), 2.6 (t, J=7.6 Hz, 2 H), 7.2-7.25 (m, 2 H), 7.3-7.35 (m, 1 H), 7.4 (s, 1 H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423158B2
Source datasetuspto-grants-2008_09
ORD IDord-6b4269c9fbc04ff79ff751fdddd84e67
Source noteuspto-grants-2008_09