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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486321Generated: October 30, 2026

2,6-Difluorobenzyl alcohol → HCID 117858216, compound

https://huagongshe.com/reaction/1486321

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Difluorobenzyl alcoholHCID 87921—
Reactant2-Fluoro-4-methoxypyridineHCID 21464361—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117858216HCID 11785821666%

Reaction Steps

To a solution of 3.5 g (27.53 mmol) of 2-fluoro-4-methoxypyridine (CAS: 175965-83-0) and 3.97 g (27.53 mmol) of 2,6-difluorobenzyl alcohol in 97 ml of dry tetrahydrofuran, cooled beforehand to 0° C., were added dropwise 27.5 ml (27.53 mmol) of a 1M solution of potassium tert-butoxide in tetrahydrofuran. The resulting mixture was stirred at room temperature for 18 hours. The solvent was evaporated off and the residue was partitioned between water and ethyl acetate. The organic phase was removed, washed with water and aqueous sodium chloride solution, dried over sodium sulphate, filtered and concentrated under reduced pressure, which gave 5.77 g (66% yield, 79% purity) of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422285B2
Source datasetuspto-grants-2016_08
ORD IDord-cd387ee420bd42c7949e98c970230938
Source noteuspto-grants-2016_08