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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677604Generated: October 30, 2026

Diethyl Ether → 2-Hydroxy-2-(3-nitrophenyl)acetonitrile

https://huagongshe.com/reaction/1677604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant3-NitrobenzaldehydeHCID 7449—
ReactantPotassium CyanideHCID 9032—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Hydroxy-2-(3-nitrophenyl)acetonitrileHCID 3277808125.4%

Reaction Conditions

Temperature10 °C

Reaction Steps

A mixture of a 10% solution of sodium bisulfite (24 g, 230 mmol) and 3-nitrobenzaldehyde (27 g, 178 mmol) was combined in a 1 L flask with 75 mL ether and 100 ml THF. The resulting reaction mixture was cooled in an ice-water bath to 10° C. and a solution of potassium cyanide (15 g, 130 mmol) in 75 mL water was added over a period of a half-hour while stirring. The reaction mixture was stirred at 15° C. for 1 hour. The organic layers were separated and the aqueous phase was extracted with ether (200 mL). The combined organic layers were dried over sodium sulfate and concentrated in vacuo to afford (3-nitrophenyl)(hydroxy)acetonitrile as a yellow oil (29 g, 163 mmol), which was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008325B2
Source datasetuspto-grants-2011_08
ORD IDord-c7355772bdb3436480f68df0397868e6
Source noteuspto-grants-2011_08