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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654615Generated: October 29, 2026

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

https://huagongshe.com/reaction/654615

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 numberUS05132469
Source datasetuspto-grants-1992_07
ORD IDord-9fe750ce504146e3841a9c63be6d7a98
Source noteuspto-grants-1992_07