Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356450Generated: October 29, 2026

Acetone → 1,5-Bis-(4-benzyloxy-phenyl)-penta-1,4-dien-3-one

https://huagongshe.com/reaction/356450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium HydroxideHCID 14798—
ReactantBenzaldehyde, 4-(phenylmethoxy)-HCID 78109—
SolventEthanolHCID 702—
Product1,5-Bis-(4-benzyloxy-phenyl)-penta-1,4-dien-3-oneHCID 471475—

Reaction Steps

The title compound was prepared as described in General Method 1 using 42.4 g (0.2 mol) 4-benzyloxybenzaldehyde, 700 mL absolute ethanol (EtOH), 5.8 g (0.1 mol) acetone and 10 mL 10% NaOH. The reaction was refluxed for 2 hours. After cooling the reaction was filtered, and the resultant solid dried. It was used without further purification in the next reaction. 1H NMR (CDCl3) δ 5.11 (s, 4 H), 6.91-7.01 (m, 6 H), 7.34-7.45 (m, 10 H), 7.57 (m, 4 H), 7.69 (d, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834506
Source datasetuspto-grants-1998_11
ORD IDord-f2f145e690574a919bfda8cca5a19c36
Source noteuspto-grants-1998_11