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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210583Generated: October 30, 2026

Potassium Cyanide → α-Hydroxy-4′-methyl[1,1′-biphenyl]-2-acetonitrile

https://huagongshe.com/reaction/2210583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant4'-Methyl[1,1'-biphenyl]-2-carbaldehydeHCID 1394009—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Productα-Hydroxy-4′-methyl[1,1′-biphenyl]-2-acetonitrileHCID 1937895284.6%

Reaction Steps

A solution of 6.0 g of potassium cyanide dissolved in 6 ml of water and a solution of 14 g of sodium hydrogensulfite dissolved in 35 ml of water were added dropwise at 0° to 5° C. to a solution of 8.00 g of 4'-methylbiphenyl-2-carbaldehyde (prepared as described in Preparation 1) dissolved in 10 ml of diethyl ether, and the resulting mixture was stirred at 5° to 10° C. for 3 hours and then at 20° C. for 30 minutes. At the end of this time, the product was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, after which the solvent was removed by evaporation under reduced pressure. The resulting residue was subjected to column chromatography through silica gel, using a 1:4 by volume mixture of ethyl acetate and hexane as the eluent, to give 7.7 g of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05459148
Source datasetuspto-grants-1995_10
ORD IDord-e99d920c3f9f430cb463cef7d3151efa
Source noteuspto-grants-1995_10