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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366781Generated: November 2, 2026

Perfluoro-1-butanesulfonyl fluoride → 3-(Nonafluorobutane-1-sulfonyloxy)-thieno[2,3-c]pyridine-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1366781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerfluoro-1-butanesulfonyl fluorideHCID 67814—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Hydroxy-thieno[2,3-c]pyridine-2-carboxylic acid ethyl esterHCID 59703877—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product3-(Nonafluorobutane-1-sulfonyloxy)-thieno[2,3-c]pyridine-2-carboxylic acid ethyl esterHCID 59703914—

Reaction Steps

To a stirred solution of 3-hydroxy-thieno[2,3-c]pyridine-2-carboxylic acid ethyl ester-(950 mg, 4.26 mmol) and DMAP (26 mg, 0.21 mmol) in DCM (12 ml) at 0° C. was added DIPEA (1.8 ml, 10.2 mmol) and nonafluorobutylsulfonyl fluoride (0.99 ml, 5.53 mmol). After 10 minutes the reaction mixture was warmed to room temperature and stirred for an additional 20 hours. The reaction mixture was diluted with DCM (30 ml) and washed with water (20 ml). The organic phase was dried over sodium sulphate, filtered and evaporated to give a yellow oil. The oil was purified by flash chromatography (Si-SPE, pentane:diethyl ether, gradient 90:10 to 65:35) to afford the title compound as a colourless oil which crystallised on standing (678 mg, 31%): LCMS (method B). RT=4.49 min, M+H+=508.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893085B2
Source datasetuspto-grants-2011_02
ORD IDord-51b6027be16940d3b31a7da3f4992b55
Source noteuspto-grants-2011_02