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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431863Generated: October 30, 2026

Pyridine → HCID 21942451, compound

https://huagongshe.com/reaction/431863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 21942652HCID 21942652—
SolventDichloromethaneHCID 6344—
ProductHCID 21942451HCID 2194245184%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of methyl 3-(aminocarbonyl)-5-propoxybenzoate (2.0 g, 8.2 mmol) in a dichloromethane (25 mL) at 0° C. was treated with pyridine (1.3 mL, 17 mmol) and then trifluoroacetic anhydride dropwise (1.4 mL, 9.9 mmol). The reaction was stirred at 0° C. for 20 minutes and then stirred overnight at ambient temperature. The reaction mixture was washed with water and saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated. Silica gel chromatography using a 40% dichloromethane/hexanes afforded 1.5 g (84%) of methyl 3-cyano-5-propoxybenzoate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660753B2
Source datasetuspto-grants-2003_12
ORD IDord-bdfec4dbd8b04a91a3f2bfe2c5dd9e73
Source noteuspto-grants-2003_12