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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610637Generated: October 27, 2026

Beta-Alanine → 2-Benzylidene-4-methyl-3-oxo-N-phenylpentanamide

https://huagongshe.com/reaction/610637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBeta-AlanineHCID 239—
ReactantBenzaldehydeHCID 240—
Reactant4-methyl-3-oxo-N-phenylpentanamideHCID 10219899—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
Product2-Benzylidene-4-methyl-3-oxo-N-phenylpentanamideHCID 5339486684.7%

Reaction Steps

A suspension of 100 kg of 4-methyl-3-oxo-N-phenyl-pentanamide (Example A) in 660 kg of hexane was treated with agitation under nitrogen with 8 kg of β-alanine, 47 kg of benzaldehyde, and 13 kg of glacial acetic acid. The resulting suspension was heated to reflux with removal of water for 20 hours. An additional 396 kg of hexane and 3 kg of glacial acetic acid was added and reflux continued with water removal for 1 hour. The reaction mixture was cooled to 20° C. to 25° C., and the product was isolated by filtration. The product was purified by slurring in hexane at 50° C. to 60° C., cooling, and filtrating. The product was slurred twice with water at 20° C. to 25° C., filtered, and dried in vacuo to yield 110 kg of 4-methyl-3-oxo-N-phenyl-2-(phenylmethylene)pentanamide, mp 143.7-154.4° C. VPC: 30 meter DB-5 capillary column 50° C. to 270° C. at 15° C./min; 19.33 minutes, 99.7% (area). GC/MS: M/Z 293 [M]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998633
Source datasetuspto-grants-1999_12
ORD IDord-f823285f5859495db632420f39e159db
Source noteuspto-grants-1999_12