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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (5-Hydroxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile | HCID 59115159 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Methylsulfonyloxyimino-5H-thiophen-2-ylidene)-phenyl-acetonitrile | HCID 54441994 | 77.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06004724 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-607654a676584d24bb1028defa5a2427 |
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| Source note | uspto-grants-1999_12 |
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