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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730203Generated: November 1, 2026

Hexane → 2-Allyl-4-fluorophenol

https://huagongshe.com/reaction/1730203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant1-Fluoro-4-(prop-2-en-1-yloxy)benzeneHCID 637342—
Product2-Allyl-4-fluorophenolHCID 11344112—

Reaction Steps

381.8 parts of oily 4-allyloxy-fluorobenzene are heated in a oil-bath for 8 hours at a temperature of about 245°-250° C. After cooling, the reaction mixture is poured onto 1200 parts of hexane. The mixture is extracted three times with sodium hydroxide solution 20% (total volume of sodium hydroxide: 2000 parts). The aqueous layer is washed with petroleum ether, acidified with 1300 parts of concentrated hydrochloric acid solution and extracted with ether. The extract is dried over calcium chloride, filtered and evaporated. The oily residue is distilled in vacuo, yielding 313.6 parts of 2-allyl-4-fluorophenol; bp.143° C at 48 mm. pressure; nD20 : 1.5225; d2020 : 1.1130.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03991202
Source datasetuspto-grants-1976_11
ORD IDord-75af140576ae4d7788cb02ee3d99c730
Source noteuspto-grants-1976_11