Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977001Generated: November 3, 2026

Allyl bromide → HCID 10921078, compound

https://huagongshe.com/reaction/1977001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTyrosolHCID 10393—
ProductHCID 10921078HCID 1092107877%

Reaction Steps

The two-step synthetic procedure of Example 1 was repeated starting with 2-(4-hydroxyphenyl)ethyl alcohol. In this case 1.2 equivalents of allyl bromide was employed in the alkylation step and the intermediate 4-allyloxyphenethyl alcohol was obtained in 77% yield following vacuum distillation (104-112° C. at 0.2 torr). Esterification of the alcohol with methacrylic acid afforded 4-allyloxyphenethyl methacrylate (AOPMA) in 88% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06231714B1
Source datasetuspto-grants-2001_05
ORD IDord-81b6d44d9a534c28af1ea5df49d96430
Source noteuspto-grants-2001_05