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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469287Generated: October 26, 2026

Hydrochloric Acid → (5-Methoxy-2-nitrophenyl)acetonitrile

https://huagongshe.com/reaction/469287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-NitroanisoleHCID 7485—
Reactant2-(4-Chlorophenoxy)acetonitrileHCID 306444—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Product(5-Methoxy-2-nitrophenyl)acetonitrileHCID 1086716839.3%

Reaction Conditions

Temperature-10 °C

Reaction Steps

24.0 g (214 mmol) potassium-tert-butoxide in 100 mL DMF were slowly added dropwise to a solution of 13.17 g (86.0 mmol) 4-nitroanisole and 18.0 g (107 mmol) 4-chlorophenoxyacetonitrile in 50 mL DMF. The reaction mixture was stirred for 30 min at −10° C. and then poured into 300 g of a 1:1 mixture of conc. HCl and ice. After extraction with EtOAc the organic phase was washed with water, dried and concentrated to dryness by rotary evaporation in vacuo with gentle heating. The residue was treated with a 1:1 mixture of PE/EtOAc and the product that crystallised out was suction filtered. After washing with a 1:1 mixture of PE/EtOAc the crystals were dried in the air. 6.5 g of the desired product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629137B2
Source datasetuspto-grants-2014_01
ORD IDord-a5d428de0d334c369a4650bf0acf66ea
Source noteuspto-grants-2014_01