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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292194Generated: October 30, 2026

4-Hydroxybenzophenone → {4-[(But-2-en-1-yl)oxy]phenyl}(phenyl)methanone

https://huagongshe.com/reaction/2292194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzophenoneHCID 14347—
Reactant2-Butene, 1-bromo-HCID 122414—
ReactantHCID 14089150HCID 14089150—
Product{4-[(But-2-en-1-yl)oxy]phenyl}(phenyl)methanoneHCID 53863387—

Reaction Steps

4-crotyloxybenzophenone was prepared from 4-hydroxybenzophenone and crotyl bromide using the procedure of Example 23. Through Claisen rearrangement it was converted into 3-(α-methyl-allyl)-4-hydroxybenzophenone. The crude product (10.1 g) was acylated (procedure of Example 1) and purified by chromatography (40:60 hexane-methylene chloride on silica gel) to produce 12.25 g (91%) of oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04801610
Source datasetuspto-grants-1989_01
ORD IDord-f9f0e0628dc8417a9036686f221bf554
Source noteuspto-grants-1989_01