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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051247Generated: October 31, 2026

Water → 4-(2-Chloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyl alcohol

https://huagongshe.com/reaction/2051247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 13911479HCID 13911479—
CatalystHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Product4-(2-Chloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyl alcoholHCID 1391148099.8%

Reaction Steps

The tetrahydropyranyl ether prepared in stage (i) (0.2 g), was dissolved in methanol (6 cm3), and to the stirred solution was added concentrated hydrochloric acid (several drops). After stirring for 6 hours, and standing for a further 14 hours, the reaction mixture was poured into water, and extracted into ethyl acetate. The organic layer was washed with water and brine, dried, and the solvent evaporated under reduced pressure to give 4-(2-chloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyl alcohol as an orange oil (0.15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05017606
Source datasetuspto-grants-1991_05
ORD IDord-2e49f30477c246838fed96c7c19a97c1
Source noteuspto-grants-1991_05