HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166376Generated: October 25, 2026
2-Thiophenecarbonitrile → HCID 178504800, compound
https://huagongshe.com/reaction/1166376
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Thiophenecarbonitrile | HCID 66087 | — |
| Reactant | 4-(Methylsulfonyl)aniline | HCID 79617 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178504800 | HCID 178504800 | — |
Reaction Steps
To a suspension of 4-(methylsulfonyl)aniline (10.4 g, 61.1 mmol) in toluene (400 ml) at 0° C., trimethylaluminum (2M solution in toluene, 46.8 ml, 91.6 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2 hours. A solution of 2-thiophenecarbonitrile (10.0 g, 91.6 mmol) in toluene (200 ml) was added over 10 minutes and the mixture was heated to 80-850° C. After 16 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue was washed with a mixture of methylene chloride/methanol and later with methanol. The combined filtrates were concentrated and the resulting yellow solid was stirred with ethyl acetate and filtered. The pale yellow solid (9.8 g, 57%) was used in the next reaction without: further purification: m.p. (DSC) 182° C. Anal. Calc'd. for C12H12N2S2O2: C, 51.41, H, 4.31, N, 9.99, S, 22.87. Found: C, 51.02, H, 4.37, N, 9.80, S, 22.93.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06613789B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-fc530aee06f84e05875a980997717084 |
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| Source note | uspto-grants-2003_09 |
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