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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623501Generated: October 31, 2026

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

https://huagongshe.com/reaction/623501

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 8742674071.8%

Reaction Steps

To a stirred suspension of sodium hydride (4.9 g, 120 mmol, 60% in oil) in N,N-dimethylacetamide (100 mL) is added dropwise 2,2,3,3,3-pentafluoropropan-1-ol (8.1 mL, 82 mmol) at 0° C. After stirring for 10 minutes, a solution of methyl 6-chloronicotinate (7.0 g, 41 mmol) in N,N-dimethylacetamide (120 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 to give 8.4 g of the title compound as a crude product (include 2,2,3,3,3-pentafluoropropyl 6-(2,2,3,3,3-pentafluoropropoxy)nicotinate as a byproduct). The residue is used for the next reaction (Step-2) without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302991B2
Source datasetuspto-grants-2016_04
ORD IDord-b9f5a949e7f5462eae306efa5f86caf3
Source noteuspto-grants-2016_04