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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623497Generated: October 29, 2026

2,2,3,3,3-Pentafluoropropanol → HCID 87426740, compound

https://huagongshe.com/reaction/623497

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,3,3,3-PentafluoropropanolHCID 9872—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 6-chloropyridine-3-carboxylateHCID 254249—
SolventDimethylacetamideHCID 31374—
ProductHCID 87426740HCID 8742674034%

Reaction Steps

To a stirred suspension of sodium hydride (3.9 g, 96 mmol, 60% in oil) in N,N-dimethylacetamide (160 mL) is added dropwise 2,2,3,3,3-pentafluoropropan-1-ol (6.4 mL, 64 mmol) at 0° C. After stirring for 10 minutes, a solution of methyl 6-chloronicotinate (5.5 g, 32 mmol) in N,N-dimethylacetamide (10 mL) is added dropwise at 0° C., and the mixture is stirred for 30 minutes at room temperature. Then, the mixture is stirred at 90° C. for 2 hours. After cooled to room temperature, 2M aqueous sodium hydroxide is added (pH is around 6). The mixture is extracted with n-hexane/ethyl acetate (1:2, 200 mL). The organic layer is washed with water, brine, and dried over sodium sulfate. The organic solvent is concentrated under reduced pressure, and the residue is purified by column chromatography on amine gel eluting with n-hexane/ethyl acetate (30:1) to give 3.1 g (34% yield) of the title compound as brown oil. MS (ESI) m/z: 286 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302991B2
Source datasetuspto-grants-2016_04
ORD IDord-836b0a1b883f464d9d37c01bb23cbd6f
Source noteuspto-grants-2016_04