HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982011Generated: October 29, 2026
m-Chloroperbenzoic acid → 5-Acetyl-2-(methanesulfinyl)thiophene-3-carbonitrile
https://huagongshe.com/reaction/982011
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 20069010 | HCID 20069010 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Acetyl-2-(methanesulfinyl)thiophene-3-carbonitrile | HCID 20068998 | — |
Reaction Steps
5.0 g of 83% m-chloroperbenzoic acid are gradually added while stirring at a temperature of 0°-5° C. in 45 minutes to a solution of 5.0 g of 2-methylthio-3-cyano-5-acetylthiophene in 500 ml of methylene chloride. After stirring for another 30 minutes at 5° C., a saturated solution of sodium bicarbonate in approximately 50 ml of water is added; the reaction mixture is then stirred for 60 minutes. The organic layer is separated, washed with water and dried. After distilling off the solvent, the desired product is obtained in a yield of 4.6 g; melting-point 150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04994485 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-dfdb45ae2dc94ab197157b2c2f99f046 |
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| Source note | uspto-grants-1991_02 |
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