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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075554Generated: October 30, 2026

Ammonium Chloride → 1-(6-(Trifluoromethyl)pyridin-3-yl)ethanol

https://huagongshe.com/reaction/2075554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant6-(Trifluoromethyl)pyridine-3-carboxaldehydeHCID 2777762—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
Product1-(6-(Trifluoromethyl)pyridin-3-yl)ethanolHCID 49760380—

Reaction Steps

To a solution of 2.0 g 6-trifluoromethyl-pyridine-3-carboxaldehyde in 20 mL of dry THF under inert atmosphere at −78° C. was added dropwise 6 ml of MeMgCl (3 M in THF). This mixture was allowed to warm up to room temperature slowly. Aqueous ammonium chloride was added to reaction mixture. The whole was extracted with ethyl acetate. The organic phase was washed with brine, dried over sodium sulphate. Purification by flash chromatography (silica, haptane/ethyl acetate) provided 0.85 g of 1-(6-trifluoromethyl-pyridin-3-yl)-ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919628B2
Source datasetuspto-grants-2011_04
ORD IDord-28ece7bb32404a82a76a3037c5fdb871
Source noteuspto-grants-2011_04