HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223471Generated: October 30, 2026
Dimethyl Sulfoxide → 4-(2-Benzoyl-4-chlorophenyl)-1H-pyrrole-3-carbonitrile
https://huagongshe.com/reaction/223471
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | 3-(2-Benzoyl-4-chlorophenyl)prop-2-enenitrile | HCID 54314020 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(2-Benzoyl-4-chlorophenyl)-1H-pyrrole-3-carbonitrile | HCID 13067086 | — |
Reaction Steps
A mixture of 10.7 g (40 mmole) of 3-(2-benzoyl-4-chlorophenyl)-2-propenenitrile, 5.3 g (38 mmole) of tosylmethyl isocyanide, 75 ml of dimethyl sulfoxide and 150 ml of ether was added dropwise to a suspension of 3.7 g (77 mmole) of 50% sodium hydride in mineral oil and 170 ml of ether. When the addition was complete stirring was continued for 2 hr. The mixture was diluted with water and the ether layer was separated. The aqueous solution was extracted with ether. The combined ether extracts were washed with water, dried over anhydrous sodium sulfate; and concentrated at reduced pressure to give a dark green oil. Purification by column chromatography (800 g silica gel; eluent 5% ether in methylene chloride) gave end product as off-white prisims, mp 175°-177°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04354973 |
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| Source dataset | uspto-grants-1982_10 |
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| ORD ID | ord-46cdd144c7f340a9b1cc59f4a05025d4 |
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| Source note | uspto-grants-1982_10 |
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