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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703299Generated: October 29, 2026

Water → HCID 637356, compound

https://huagongshe.com/reaction/703299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Tert-ButylphenolHCID 6923—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
ProductHCID 637356HCID 63735681.3%

Reaction Steps

To a stirred solution of o-(t-butyl)-phenol (11.3 g; 75 mmol) in acetone (150 ml) is added allyl bromide (10.9 g, 1.2 equiv.) and anhydrous K2CO3. After stirring 18 hr at reflux, the reaction is added to water (200 ml) and extracted with 3×150 ml portions of petroleum ether. The combined organic layers are dried (MgSO4), filtered, and concentrated in vacuo to give the crude product, which is purified by silica gel (sg) chromatography (hexane elution) to yield 1-prop-2-enyloxy-2-t-butylbenzene (11.6 g; 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04982006
Source datasetuspto-grants-1991_01
ORD IDord-47e8c47cc7324c9a94125e47d839c6cd
Source noteuspto-grants-1991_01