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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330627Generated: October 30, 2026

Beta-Alanine → HCID 14539520, compound

https://huagongshe.com/reaction/330627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBeta-AlanineHCID 239—
ReactantBenzeneHCID 241—
ReactantEthyl cyanoacetateHCID 7764—
Reactant4,4'-DifluorobenzophenoneHCID 9582—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 14539520HCID 1453952056.3%

Reaction Steps

A mixture of 20.0 g (92 mmoles) of 4,4'-difluorobenzophenone, 11.0 g (97 mmoles) of ethyl cyanoacetate in a mixed solvent of 100 mL of dry benzene and 20 mL of glacial acetic acid containing a catalytic amount of β-alanine (0.9 g) was refluxed with separation of water using a Dean-Stark water trap. Separation of water was rapid during the first 2 hours (0.4 mL aqueous layer collected) but slower afterward. Azeotropic distillation was continued for a period of 14 days. Analytical TLC eluted with 10% EtOAc in hexanes (v/v) (Merck plate, 0.25 mm Silica gel-F) showed two spots at Rf =0.2 (desired product) and at Rf =0.45 (4,4'-difluorobenzophenone starting material). Crude reaction mixture was washed with water (40 mL×2), and the combined aqueous washes were extracted with EtOAc (150 mL×2). The organic layers were combined, dried over MgSO4 and concentrated under reduced pressure to crystallize the product as pale cubic crystals. The crude product was collected, washed with 1:1 EtOAc in hexanes (v/v) then recrystallized from 8:1 (hexanes:ethyl acetate v/v) to give 16.2 g (56.3%) of analytical pure title compound; m.p.=114°-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04897490
Source datasetuspto-grants-1990_01
ORD IDord-52954f71070c402faef62c69f8084606
Source noteuspto-grants-1990_01