Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869150Generated: October 31, 2026

Potassium tert-butoxide → 1,3-Dichloro-5-(3,3-dichloro-allyloxy)-2-[4-(4-fluoro-phenyl)-pent-4-enyloxy]-benzene

https://huagongshe.com/reaction/1869150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-[2,6-Dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-1-(4-fluoro-phenyl)-butan-1-oneHCID 86613088—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTolueneHCID 1140—
Product1,3-Dichloro-5-(3,3-dichloro-allyloxy)-2-[4-(4-fluoro-phenyl)-pent-4-enyloxy]-benzeneHCID 57985792—

Reaction Conditions

Temperature80 °C

Reaction Steps

84 mg of potassium tert-butylate and 236 mg of methyltriphenylphosphonium bromide are stirred in 6 ml of toluene for 3 hours at 80° C. 200 mg of 4-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-1-(4-fluoro-phenyl)-butan-1-one in 2 ml of toluene are then added and the mixture is stirred for a further 2 hours at 80° C. The reaction mixture is cooled and filtered and the filtrate is concentrated. After purification over silica gel, the title compound is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638514B2
Source datasetuspto-grants-2009_12
ORD IDord-5f4aced13c134e37b8a19880b9a4e70b
Source noteuspto-grants-2009_12