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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495454Generated: October 30, 2026

Sodium Cyanide → (2-Methoxy-5-nitrophenyl)acetonitrile

https://huagongshe.com/reaction/495454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant2-(Bromomethyl)-1-methoxy-4-nitrobenzeneHCID 77516—
SolventEthanolHCID 702—
Product(2-Methoxy-5-nitrophenyl)acetonitrileHCID 12701835—

Reaction Steps

2-Bromomethyl-1-methoxy-4-nitro-benzene (25 g) was dissolved in warm EtOH (45 mL) and stirred while slowly adding a solution of NaCN (6.0 g in 12 mL water) at 70° C. After the addition was complete, the reaction was stirred at 70° C. for 90 min. The inorganic solid, which separated on cooling, was collected and washed well with CH3CN. The CH3CN filtrate was filtered again giving further inorganic solid, and again washed with CH3CN. The final CH3CN filtrate was evaporated giving a red-brown solid. This solid was triturated with CH2Cl2 until the washings were colorless. Evaporation of the CH2Cl2 filtrate gave (2-methoxy-5-nitrophenyl)-acetonitrile as a red-brown solid, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939874B2
Source datasetuspto-grants-2005_09
ORD IDord-e7277dcabd3448eeb64dc995d5a53cc2
Source noteuspto-grants-2005_09