Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493431Generated: October 31, 2026

Phenol → HCID 57057502, compound

https://huagongshe.com/reaction/1493431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 3533755HCID 3533755—
ReactantHCID 11171268HCID 11171268—
SolventAcetoneHCID 180—
ProductHCID 57057502HCID 57057502—

Reaction Steps

O-propenylphenol (67 g) was added to a stirred suspension of potassium carbonate (138 g) in dry acetone. Allyl bromide (67 g) was then added dropwise over about 20 minutes and the stirred mixture was heated under reflux for 4 hours. After this time, gas liquid chromatography indicated that the phenol had been converted to about 95% of a mixture of cis and trans 2-allyloxy-1-propenylbenzene. The mixture was filtered and the solvent removed under reduced pressure. The residue was vacuum distilled and yielded 58.9 g of almost pure 2-allyloxy-1-propenylbenzene which was identified spectroscopically. [b.p. 64-88° C. at 0.6 mbar].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021512
Source datasetuspto-grants-1991_06
ORD IDord-3de632b9268c44fa87b847a46594feba
Source noteuspto-grants-1991_06