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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366772Generated: October 31, 2026

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

https://huagongshe.com/reaction/1366772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerfluoro-1-butanesulfonyl fluorideHCID 67814—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Hydroxy-thieno[3,2-c]pyridine-2-carboxylic acid ethyl esterHCID 59703916—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product3-(Nonafluorobutane-1-sulfonyloxy)-thieno[3,2-c]pyridine-2-carboxylic acid ethyl esterHCID 59703908—

Reaction Steps

To a stirred solution of 3-hydroxy-thieno[3,2-c]pyridine-2-carboxylic acid ethyl ester (1.3 g, 5.82 mmol) and DMAP (35 mg, 0.29 mmol) in DCM (10 ml) at 0° C. was added DIPEA (2.5 ml, 14.0 mmol) and nonafluorobutylsulfonyl fluoride (1.36 ml, 7.56 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 (50 ml) and washed with water (30 ml). The organic phase was isolated, dried over sodium sulphate, filtered and evaporated to give a brown oil. The oil was purified by flash chromatography (Si-SPE, pentane:diethyl ether, gradient 100:0 to 70:30) to afford the title compound as a colourless oil which crystallised on standing (420 mg, 14%). LCMS (method B): RT=4.46 min, M+H+=508.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893085B2
Source datasetuspto-grants-2011_02
ORD IDord-e98db72ae9e64c35b94c615af2a9ae20
Source noteuspto-grants-2011_02