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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085715Generated: November 2, 2026

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

https://huagongshe.com/reaction/1085715

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 numberUS05010200
Source datasetuspto-grants-1991_04
ORD IDord-edd957f24ef04014907ccb6f1d44fd79
Source noteuspto-grants-1991_04