HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978733Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 23050233, compound
https://huagongshe.com/reaction/978733
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 23050232 | HCID 23050232 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23050233 | HCID 23050233 | — |
Reaction Steps
A mixture of powdered potassium hydroxide (12.36 g) and dimethylsulphoxide (100 ml) was stirred at room temperature for 5 min. then treated with 5,6 -dihydroxy-benzo[b]thiophene-2-carbonitrile (5.26 g). After 1 minute di-iodomethane (4.4 ml) was added and the suspension was stirred at room temperature for 75 minutes, then more di-iodomethane (2.2 ml) was added. After a further 30 minutes the reaction was poured into water (500 ml) and extracted with ethyl acetate (2×100 ml). The organic extracts were combined, washed with 2MHCl and saturated brine, then dried and evaporated to give a brown crystalline residue. The crude product was suspended in hot dichloromethane (200 ml), filtered, and the filtrate was passed through a column of silica gel (0.2-0.5 mm, Merck, 25 g). The appropriate fractions were combined and evaporated to dryness to give a white solid (3.4 g). Crystallisation from acetone/ether afforded pure thieno[2,3-f]-1,3-benzodioxole-6-carbonitrile, m.p. 179°-180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04665206 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-05cb7776de1e41acb9e9ede39bdf6e33 |
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| Source note | uspto-grants-1987_05 |
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