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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579862Generated: October 31, 2026

Allyl Alcohol → HCID 21288544, compound

https://huagongshe.com/reaction/579862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
ReactantSodium HydroxideHCID 14798—
ReactantBenzene, 1-(chloromethyl)-4-(1,1-dimethylethyl)-HCID 88198—
CatalystTetrabutylammonium ChlorideHCID 70681—
ProductHCID 21288544HCID 21288544—

Reaction Steps

88 g (1.1 mol) of 50% sodium hydroxide solution are treated with 4.6 g (0.016 mol) of tetrabutylammonium chloride. At a temperature of 35° C. there is added dropwise within about 20 minutes while stirring well a mixture of 182.5 g (1.0 mol) of p-tert-butylbenzyl chloride and 61.5 g (1.06 mol) of allyl alcohol. The temperature is held at <70° C., which is accomplished if necessary by slight cooling. The mixture is stirred well at 70° C. for a further 12 hours. After cooling, the reaction mixture is washed twice with dilute hydrochloric acid. 204 g of practically pure p-tert-butylbenzyl allyl ether are obtained. The substance can be used without distillation for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04749815
Source datasetuspto-grants-1988_06
ORD IDord-8b46b3848e504b9f8cd7969197762cfe
Source noteuspto-grants-1988_06