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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240997Generated: October 27, 2026

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

https://huagongshe.com/reaction/2240997

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, 2H), 2.1-2.2 (m, 2H), 2.6 (t, J=7.6 Hz, 2H), 7.2-7.25 (m, 2H), 7.3-7.35 (m, 1H), 7.4 (s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723368B2
Source datasetuspto-grants-2010_05
ORD IDord-7fe1c1adb65941efaf428139f6661ff6
Source noteuspto-grants-2010_05