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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296604Generated: October 30, 2026

Allyl Alcohol → HCID 527701, compound

https://huagongshe.com/reaction/2296604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
ReactantHexaneHCID 8058—
Reactant4-Chlorobutanoic acidHCID 12300—
SolventWaterHCID 962—
ProductHCID 527701HCID 52770179%

Reaction Steps

To a mixture of 4-chlorobutyric acid (48 ml; 0.48 mole), allyl alcohol (200 ml) and hexane (1.2 l) p-toluenesulfonic acid (16.0 g; 0.08 mole) was added. The obtained mixture was heated for 5 hours at reflux temperature in such a way that water was simultaneously removed with Dean-Stark apparatus (Vogel's Textbook of Practical Organic Chemistry, Fourth Ed., Longman, London, 1978, p. 411). The mixture was then cooled to room temperature and shaken with 7% aqueous sodium hydrogencarbonate solution (2×500 ml). The obtained solution was dried with magnesium sulfate and after the filtration of the drying agent hexane was evaporated. The crude residue was distilled under reduced pressure 10 mbar at the temperature of 95° C. and the title compound (61.2 g; 79%) was obtained in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489318B1
Source datasetuspto-grants-2002_12
ORD IDord-94d63f3bf0544516b297b5d11806b7ff
Source noteuspto-grants-2002_12