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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677602Generated: November 4, 2026

3-Nitrobenzaldehyde → 2-Hydroxy-2-(3-nitrophenyl)acetonitrile

https://huagongshe.com/reaction/1677602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
ReactantPotassium CyanideHCID 9032—
ReactantSodium BisulfiteHCID 23665763—
SolventDiethyl EtherHCID 3283—
Product2-Hydroxy-2-(3-nitrophenyl)acetonitrileHCID 327780887.4%

Reaction Conditions

Temperature10 °C

Reaction Steps

A mixture of m-nitrobenzaldehyde (27.0 g, 178.7 mmol) and a 10% solution of 24 g of sodium bisulfite was placed in a 2 liter flask and 75 mL of ether was added. The resulting mixture was cooled in an ice-bath to 10° C. and potassium cyanide (15.0 g, 230.3 mmol) in a 20% solution was added over a period of 30 minutes. The mixture was stirred for another 30 minutes after the addition of the potassium cyanide. The ether layer was separated and the aqueous layer was extracted with ether. The combined organic layers were dried over sodium sulfate and concentrated in vacuo to afford 27.81 g (87%) of α-hydroxy-3-nitrobenzeneacetonitrile, a compound of formula (Q), as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008325B2
Source datasetuspto-grants-2011_08
ORD IDord-b5e0dd8d9592477aa78d153a83cf1010
Source noteuspto-grants-2011_08