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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892928Generated: October 30, 2026

2,3,6-Trifluorobenzonitrile → 3,6-Difluoro-2-methoxybenzonitrile

https://huagongshe.com/reaction/1892928

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,6-TrifluorobenzonitrileHCID 145622—
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product3,6-Difluoro-2-methoxybenzonitrileHCID 4579073391%

Reaction Steps

Methanol (600 mL) was treated portionwise with sodium (Alfa, 16.1 g, 0.702 gatoms, 1.05 equiv.). The sodium methoxide solution was cooled to room temperature and added dropwise to a solution of 2,3,6-trifluorobenzonitrile (Matrix, 105 g, 0.699 mol) in methanol (600 ml) at room temperature. After addition was complete the mixture was stirred for 1 hour at room temperature before removing the methanol under reduced pressure. The residue was partitioned between diethyl ether (500 ml) and water (500 mL). The organic layer was removed, dried over MgSO4, filtered and evaporated to give the crude product. This was purified by distillation using a 6″ vigreux column @ 20 mmHg, oil bath 160° C., head temp 120° C. to give the title compound as a white solid (108 g, 91%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507543B2
Source datasetuspto-grants-2013_08
ORD IDord-2efefe333c3c4888aa2df9c98c7a0a43
Source noteuspto-grants-2013_08