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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232867Generated: October 27, 2026

Acetic Acid → 2-Cyano-6-methylbenzoic acid

https://huagongshe.com/reaction/232867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
Reactant6-Methylanthranilic acidHCID 151210—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product2-Cyano-6-methylbenzoic acidHCID 57022117—

Reaction Steps

Under ice cooling and stirring, 1.5 g of sodium nitrite dissolved in 2 ml of water was added dropwise over 1.5 hours to 3 g of 3-amino-o-toluic acid dissolved in a mixed solution of 8 ml of acetic acid, 8.3 g of sulfuric acid and 6.5 ml of water. After 3.2 ml of acetic acid, 0.4 g of sulfuric acid and 5.6 ml of water were added to the reaction mixture, the mixture was filtered and the reaction filtrate was adjusted. On the other hand, 6.5 g of potassium cyanide dissolved in 12.7 ml of water was added dropwise to 5.9 g of copper sulfate.pentahydrate dissolved in 12.7 ml of water at room temperature under stirring and 21.5 g of sodium hydrogen carbonate and 70 ml of toluene were added to the mixture. Under ice cooling and stirring, the above reaction filtrate was added dropwise to this 10 reaction mixture over 1 hour and then the mixture was stirred at 80° C. for 30 minutes. After completion of the reaction, the reaction mixture was adjusted to about pH 3 with 1N-hydrochloric acid, crystals precipitated were extracted with ethyl acetate and the organic layer was washed with a saturated saline solution and then dried over anhydrous sodium carbonate. The solvent was removed to obtain 3.8 g of the title compound. Mass (CI); m/z=162 (M+ +1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591752
Source datasetuspto-grants-1997_01
ORD IDord-f2c49aa6af8e4205899da96c87f76d5c
Source noteuspto-grants-1997_01