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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527466Generated: November 4, 2026

Hydrochloric Acid → [3-Fluoro-2-(trifluoromethyl)pyridin-4-yl]methanol

https://huagongshe.com/reaction/1527466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Fluoro-2-(trifluoromethyl)isonicotinic acidHCID 26596489—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product[3-Fluoro-2-(trifluoromethyl)pyridin-4-yl]methanolHCID 68283421—

Reaction Steps

Carbonyldiimidazole (1.16 g, 7.17 mmol) was added to a solution of 3-fluoro-2-trifluoromethyl-isonicotinic acid (1.00 g, 4.78 mmol) in THF (13.7 mL). The reaction mixture was stirred at RT overnight and was then added to a cold (0° C.) solution of NaBH4 (0.905 g, 23.9 mmol) in water (34.2 mL). The mixture was stirred for 10 min at 0° C., and 1M HCl was then added carefully (caution: H2 evolving). Volatiles were removed under reduced pressure, and the residue was dissolved in saturated aqueous NaHCO3. The mixture was extracted repeatedly with CH2Cl2, the combined organics were dried (phase separator) and concentrated in vacuo. Purification by flash column chromatography on silica gel (eluent gradient: c-hexane/EtOAc 1:1 to 0:1) afforded the title compound as a yellow oil. TLC, Rf (c-hexane/EtOAc 1:1)=0.27; MS (LC/MS): 196.0 [M+H]+; tR (HPLC conditions b): 2.62 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-692b8e5207b6449ea85f4a2644e2e755
Source noteuspto-grants-2015_07