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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 4'-Methyl[1,1'-biphenyl]-2-carbaldehyde | HCID 1394009 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | α-Hydroxy-4′-methyl[1,1′-biphenyl]-2-acetonitrile | HCID 19378952 | 84.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05459148 |
|---|
| Source dataset | uspto-grants-1995_10 |
|---|
| ORD ID | ord-e99d920c3f9f430cb463cef7d3151efa |
|---|
| Source note | uspto-grants-1995_10 |
|---|