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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080601Generated: November 1, 2026

Acetic Acid → HCID 67102427, compound

https://huagongshe.com/reaction/2080601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzylamineHCID 7504—
ReactantMethyl cyanoacetateHCID 7747—
Reactant1-(4-Fluoro-2-methoxyphenyl)ethan-1-oneHCID 142887—
SolventTolueneHCID 1140—
ProductHCID 67102427HCID 6710242795.6%

Reaction Steps

To a round bottom flask fitted with a Dean-Stark trap was added a mixture of 19.54 g (116 mmol) of 4-fluoro-2-methoxyacetophenone, 15.29 mL (174 mmol) of methyl cyanoacetate, 1.42 mL (13 mmol) of benzylamine, and 6.6 mL of acetic acid in 170 mL of toluene and the mixture was warmed to reflux. The reaction was monitored by TLC (EtOAc-hexanes, 2:8). After 18 hours, the reaction was then cooled and concentrated in vacuo to afford a dark, orange oil. The crude oil was distilled at 130° C. under vacuum (Kugelrohr) to remove unreacted 4-fluoro-2-methoxyactophenone. The crude product was then passed through a pad of silica gel using a 10% EtOAc in a 1:1 mixture of dichloromethane in hexanes to afford 27.64 g (95%) of 2-cyano-3-(4-fluoro-2-methoxyphenyl)but-2-enoic acid methyl ester as a light orange oil which was a mixture of geometric isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932392B2
Source datasetuspto-grants-2011_04
ORD IDord-6a5097954d5f450e895726a9551da158
Source noteuspto-grants-2011_04