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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658461Generated: October 28, 2026

Benzyl Alcohol → 5-(Benzyloxy)-2-nitrobenzonitrile

https://huagongshe.com/reaction/658461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-2-nitrobenzonitrileHCID 3756467—
SolventDimethylformamideHCID 6228—
Product5-(Benzyloxy)-2-nitrobenzonitrileHCID 2182487275.6%

Reaction Steps

A mixture of 5-fluoro-2-nitrobenzonitrile (15 g, 90 mmol), benzyl alcohol (10.8 g, 100 mmol) and potassium carbonate (18.7 g, 135 mmol) in DMF (20 ml) was stirred at room temperature for 60 h. Water (60 ml) was added to the reaction, and the resultant yellow precipitate out filtered, washed with water, and dried under reduced pressure to provide 17.3 g (75.4%) of 5-benzyloxy-2-nitrobenzonitrile. The compound was used directly for the next step without further purification. MS GC-MS M+=211, RT=6.15 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076488B2
Source datasetuspto-grants-2011_12
ORD IDord-6b15739c0192446f9f08a06a09ad8fbf
Source noteuspto-grants-2011_12