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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1153887Generated: October 31, 2026

Benzaldehyde → 2-Methylcinnamic aldehyde

https://huagongshe.com/reaction/1153887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantPropanalHCID 527—
ReactantSodium HydroxideHCID 14798—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-Methylcinnamic aldehydeHCID 755738.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

Propionaldehyde (87 gms 15 moles) was added at 50° C. over a period of 5 hours to a stirred mixture of benzaldehyde (318 gms, 3 moles), methanol (500 mls), water (500 mls) and sodium hydroxide (25 gms). After a further 1 hour stirring at 50° C., the reaction mixture was brought to neutrality with acetic acid and the methanol fractionated out of the reaction. The organic layer was then separated from the aqueous layer and fractionated to recover the excess of benzaldehyde (109 gms, b.pt. 36°-40° C./2 mm Hg) and obtain the -methylcinnamaldehyde (167 gms, b.pt. 100°-102° C./2 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04486607
Source datasetuspto-grants-1984_12
ORD IDord-f75f835ba2bb44e7b4ccddff118281b7
Source noteuspto-grants-1984_12