Sodium Cyanide → 4-Hydroxybenzyl cyanide
Reaction equation
[C-:1]#[N:2].[Na+].Cl[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[CH:8][CH:7]=1>CO>[C:1]([CH2:5][C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[CH:8][CH:7]=1)#[N:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of p-chloromethyl phenol in acetonitrile (Example 12) was reacted with equimolar sodium cyanide in excess methanol (800 parts methanol/mole sodium cyanide) and the reaction mixture was refluxed for one hour. The oil after solvent evaporation (washed as in Experiment 18) was fractionated to yield 45% of α-cyano-p-cresol (b.p. 50°-155°/1 mm. of mercury; M.P. 68°-70°). Infrared spectra confirmed the identity of the product.
Workup
- temperaturethe reaction mixture was refluxed for one hour
- customThe oil after solvent evaporation (washed as in Experiment 18)
Sources & evidence
- ORD record
- ord-6627a186138b4c15b087c47cc03bf7fe
- Source dataset
- uspto-grants-1976_09
- Patent number
- US03983178
Reaction notes
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