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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397263Generated: October 29, 2026

HCID 67325611, compound → HCID 67324020, compound

https://huagongshe.com/reaction/1397263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67325611HCID 67325611—
ReactantHCID 178418260HCID 178418260—
SolventDimethylformamideHCID 6228—
ProductHCID 67324020HCID 6732402039%

Reaction Steps

The product methyl 3-bromo-5-ethylbenzoate (0.9 g, 3.7 mmol) was dissolved in dry DMF (50 mL) and copper cyanide (0.84 g, 9.43 mmol) was added. The reaction mixture was heated to 150° C. under argon atmosphere for 12 h (monitored by TLC; petroleum ether/EtOAc 9:1). The reaction mixture was allowed to come to room temperature and then quenched with saturated ammonium chloride solution. The reaction mixture was diluted with EtOAc and filtered through a Celite bed. The filtrate was diluted with EtOAc and the organic layer was washed with water and brine. The solvent was evaporated under reduced pressure. The crude product was purified by column chromatography (silica 60-120 mesh, eluent 5% EtOAc in petroleum ether) to get methyl 3-cyano-5-ethylbenzoate (0.27 g, yield 39%) as colorless liquid, which was carried through without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-c200f8db42a84c4b8bd7b7787641c199
Source noteuspto-grants-2014_12