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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425771Generated: October 31, 2026

Potassium Hydroxide → HCID 16726889, compound

https://huagongshe.com/reaction/425771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantAmmonium HydroxideHCID 14923—
Reactant4'-(Aminomethyl)[1,1'-biphenyl]-2-carbonitrile--hydrogen chloride (1/1)HCID 23655859—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 16726889HCID 1672688984.1%

Reaction Conditions

Temperature72.5 °C

Reaction Steps

4-Aminomethyl-2′-cyanobiphenyl hydrochloride (XVII) (100 g, 0.408 mole) was suspended in a mixture of water (500 ml) and methylene chloride (200 ml) at 25-30° C. and adjusted the pH to 9.0-9.5 with ammonium hydroxide (65 ml, 20% w/w) at 25-30° C. to get a clear solution. Organic layer was separated, washed with water (100 ml) and dried over sodium sulfate. Thereafter, organic layer was concentrated at below 60° C. and tert.butanol (300 ml) was added to the residue. The reaction mass was heated to 70-75° C. Thereafter, powdered potassium hydroxide (32.35 g, 0.491 mole) was added and heated to reflux for completion of the reaction. Water (400 ml) was added and aqueous layer was separated and extracted with methylene chloride (500 ml). The combined organic layer was washed with water (200 ml) and dried over sodium sulfate. Methylene chloride solution was cooled to 2-5° C. and the pH adjusted to 1.2-1.4 with hydrochloric acid. The precipitated product was stirred for one hour and filtered, washed with methylene chloride to afford the title compound as white powder (90 g, 84.1% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106216B2
Source datasetuspto-grants-2012_01
ORD IDord-0a8955554706472095e2a500951e9319
Source noteuspto-grants-2012_01