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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717921Generated: October 29, 2026

Acetic Acid → 4-Cyanobenzaldehyde

https://huagongshe.com/reaction/717921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl 4-aminobenzoateHCID 12082—
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantCyano-borohydrideHCID 498716—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product4-CyanobenzaldehydeHCID 6604230%
ProductHCID 43087792HCID 43087792—

Reaction Steps

A solution of methyl 4-aminobenzoate (0.2 g, 1.323 mmol) and 4-formylbenzonitrile (0.177 g, 1.350 mmol) in methanol (2 ml) and dichloromethane (4 ml) was treated with acetic acid (0.379 ml, 6.62 mmol) followed by MP-cyanoborohydride (1.151 g, 2.65 mmol) and the reaction was slowly stirred at room temperature. After 16 hours, the mixture was filtered and concentrated and the concentrate was partitioned between 2 N sodium hydroxide and dichloromethane. The organic phase was concentrated to give the title compound with 30% of remaining 4-formylbenzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193723B2
Source datasetuspto-grants-2015_11
ORD IDord-6ecaefaeab834c7cb7968d1bc9816acf
Source noteuspto-grants-2015_11