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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34608Generated: October 28, 2026

Hydrochloric Acid → Z-4-(3-chloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyl alcohol

https://huagongshe.com/reaction/34608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 54011856HCID 54011856—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductZ-4-(3-chloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyl alcoholHCID 13911478—

Reaction Steps

The tetrahydropyranyl ether prepared in stage (ii) was dissolved in methanol (30 cm3), and to the stirred solution was added a catalytic amount of concentrated hydrochloric acid. After stirring for two hours, the reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed and dried, and the solvent evaporated under reduced pressure to give Z-4-(3-chloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyl alcohol (0.6 g) as a colourless oil, which solidified on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04762835
Source datasetuspto-grants-1988_08
ORD IDord-df994d04c0054c998bbdfece7eb174fb
Source noteuspto-grants-1988_08