Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292193Generated: October 30, 2026

4-Hydroxybenzophenone → [4-Hydroxy-3-(prop-2-en-1-yl)phenyl](phenyl)methanone

https://huagongshe.com/reaction/2292193

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzophenoneHCID 14347—
Reactant4-AllyloxybenzophenoneHCID 257910—
Product[4-Hydroxy-3-(prop-2-en-1-yl)phenyl](phenyl)methanoneHCID 25791247%

Reaction Steps

4-hydroxybenzophenone (25 g) was converted to 4-allyloxybenzophenone (29.2 g, yellow solid) by the procedure of Example 23. Claisen rearrangement using that procedure gave 13.5 g (47%) of desired 3allyl-4-hydroxybenzophenone, the balance being recovered. Finally, acylation of 3-allyl-4-hydroxybenzophenone (5.9 G) according to general procedure of Example 1 produced 6.9 g (86%) of product as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04801610
Source datasetuspto-grants-1989_01
ORD IDord-64e158f082a94f37b08cdc212ec780e4
Source noteuspto-grants-1989_01