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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176963Generated: October 30, 2026

1-Phenylethanol → HCID 66924294, compound

https://huagongshe.com/reaction/2176963

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylethanolHCID 7409—
ReactantBenzonitrileHCID 7505—
ReactantSodium hydrideHCID 24758—
Reactant2,6-DifluorobenzonitrileHCID 74695—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66924294HCID 6692429486.4%

Reaction Steps

Sodium hydride (60%; 316 mg; 7.9 mmol) was suspended in DMF and cooled to 0° C. sec-Phenethyl alcohol (966 mg; 7.9 mmol) was dissolved in DMF and added dropwise to the sodium hydride mixture. The solution was allowed to warm to room temperature and stirred for 1 hour. The solution was then cooled to 0° C. 2,6-Difluorobenzonitrile (1 g; 7.2 mmol) in DMF was cooled to 0° C. and the alcohol mixture was added dropwise to the benzonitrile solution and stirred for 2 hours. The solution was poured over 100 mL of cooled water. The solution was stored in the refrigerator for 3 hours and the solid was collected by filtration and dried under vacuum to yield 1.50 grams of 2-fluoro-6-(1-phenylethoxy)benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067897B2
Source datasetuspto-grants-2015_06
ORD IDord-bb7540e1a21a48f69ac0da95239ef8f8
Source noteuspto-grants-2015_06