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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648769Generated: October 25, 2026

Pyridine → alpha-(4-Acetoxybenzenesulfonyloxyimino)thien-2-ylacetonitrile

https://huagongshe.com/reaction/648769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiethyl EtherHCID 3283—
Reactant4-(Chlorosulfonyl)phenyl acetateHCID 12925710—
ReactantAlpha-Oximino-2-ThienylacetonitrileHCID 73667355—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Productalpha-(4-Acetoxybenzenesulfonyloxyimino)thien-2-ylacetonitrileHCID 5449158053.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

200 mg of 4-dimethylaminopyridine and 6.2 g (0.08 mole) of pyridine are added to a solution of 12 g (0.08 mole) of α-hydroxyiminothien-2-ylacetonitrile (3b) in 75 ml of tetrahydrofuran. With cooling to 0° C., a solution of 18.5 g (0.08 mole) of 4-acetoxybenzenesulfonyl chloride (3a) in 30 ml of tetrahydrofuran is added dropwise. The reaction mixture is stirred for 16 hours at room temperature, and 100 ml of diethyl ether are subsequently added. The precipitated salts are removed by filtration and the solution is concentrated by evaporation. The residual crude product is recrystallised from hexane/ethyl acetate, affording 15 g of crystals with a melting point of 114°-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04736055
Source datasetuspto-grants-1988_04
ORD IDord-6e35bdfa6f57408fb75bc914e9662299
Source noteuspto-grants-1988_04