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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612358Generated: October 25, 2026

Water → (5-Methylsulfonyloxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile

https://huagongshe.com/reaction/612358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(5-Hydroxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrileHCID 59115159—
SolventTetrahydrofuranHCID 8028—
Product(5-Methylsulfonyloxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrileHCID 5444199477.2%

Reaction Steps

5 g (22 mmol) of (5-Hydroxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile are dissolved in 50 ml of THF and cooled in an ice bath. After adding 4.6 ml (33 mmol) of triethylamine to the solution, 1.9 ml (24 mmol) of methanesulfonyl chloride are added dropwise, keeping the temperature below 5° C. The reaction mixture is stirred while cooling in an ice bath for 30 min. The reaction mixture is poured into 200 ml of water, and extracted with ethyl acetate. The organic phase is washed with hydrochloric acid solution and sodium chloride solution. The organic phase is dried over MgSO4, the solvent is distilled off, and the residue is purified by recrystallization from toluene. 5.2 g (77%) of (5-Methylsulfonyloxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile are obtained in the form of greenish brown crystals having a melting point of 160-162° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06004724
Source datasetuspto-grants-1999_12
ORD IDord-607654a676584d24bb1028defa5a2427
Source noteuspto-grants-1999_12