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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288492Generated: October 26, 2026

Water → 4-tert-Butyl-3-hydroxy-2,6-xylylacetonitrile

https://huagongshe.com/reaction/1288492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CyanideHCID 9032—
Reactant6-tert-Butyl-3-(chloromethyl)-2,4-dimethylphenolHCID 90131—
SolventDimethylformamideHCID 6228—
Product4-tert-Butyl-3-hydroxy-2,6-xylylacetonitrileHCID 108756—

Reaction Steps

To 41 grams of potassium cyanide dispersed in 300 ml of N,N-dimethylformamide, was slowly added a solution of 97.2 grams of the compound of Example 1, the reaction temperature rising from 25° to 35° C. The reaction mixture was then heated at 70° to 75° for 7 1/2 hours. Since a sample analyzed after 7 hours reaction time indicated that some unreacted staring 6-tert.-butyl-3-chloromethyl-2,4-dimethyl-phenol remained unreacted, an additional 13.7 grams of potassium cyanide was added and the reaction mixture heated for an additional 2 hours at 60° to 65° C. The reaction mixture was poured on crushed ice, and water added to made the total volume 1.8 liters. The mixture was stirred until the ice melted, the aqueous solid dispersion was filtered by suction, and the filtercake washed well with water. The filtercake was taken up in a toluene-benzene mixture, the resulting solution being successively washed with water, 6N aqueous hydrochloric acid and dried over anhydrous sodium sulfate. After removal of the drying agent by filtration and treating the clear filtrate with activated charcoal, the solvent was evaporated at reduced pressures. The resulting residue was allowed to crystallize from toluene yielding white crystals melting at 134° to 139°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03988363
Source datasetuspto-grants-1976_10
ORD IDord-76ab26853c63424fa7d5bd7f05d4333a
Source noteuspto-grants-1976_10