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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287417Generated: October 26, 2026

Benzaldehyde → Ccris 2231

https://huagongshe.com/reaction/1287417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant4'-MethoxyacetophenoneHCID 7476—
ReactantSodium HydroxideHCID 14798—
SolventEthanolHCID 702—
ProductCcris 2231HCID 9285391%

Reaction Steps

50.1 g. (0.333 m) 4-methoxyacetophenone and 35.4 g (0.333 m) benzaldehyde were combined in a 500 ml Erlenmeyer flask, with the 4-methoxyacetophenone being previously melted. Then 80 ml 5N NaOH solution (appr.) (1.2 × 0.333 m) was added to the mixture. Approximately 40 ml absolute ethanol was added to the stirred mixture in small portions to keep the mixture homogeneous. It was let stir at room temperature overnight, and a solid white cake resulted. The solid was filtered, washed with water, and then recrystallized from methanol/water to give 72.3 g (91%) of 1-(4-methoxyphenyl)-3-phenyl-2-propen-1-one. 10 g (0.0420 m) of this compound and 160 mg Pd on C (10%) were combined with about 200 ml ethyl acetate and placed under 1 atm of hydrogen. Upon stirring, the mixture absorbed 950 ml H2 (calc. 940 ml) and stopped. The reaction mixture was filtered and the clear solution was concentrated to obtain 9.8 g (98%) of 1-(4-methoxyphenyl)-3-phenyl-1-propanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03984501
Source datasetuspto-grants-1976_10
ORD IDord-7b6aeeb477794a78b89206bf7879b985
Source noteuspto-grants-1976_10