HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296271Generated: October 29, 2026
Dimethyl Sulfoxide → HCID 13067089, compound
https://huagongshe.com/reaction/2296271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(1-Isocyanoethanesulfonyl)-4-methylbenzene | HCID 11052885 | — |
| Reactant | 3-[4-Chloro-2-(2-fluorobenzoyl)phenyl]prop-2-enenitrile | HCID 53972742 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13067089 | HCID 13067089 | — |
Reaction Steps
A mixture of 34.5 g (121 mmole) of 3-[2-(2-fluorobenzoyl)-4-chlorophenyl]-2-propenenitrile, 25.3 g (121 mmole) of 1-tosylethyl isocyanide, 200 ml of dimethyl sulfoxide and 400 ml of ether was added dropwise to a suspension of 8.9 g (184 mmole) of 50% sodium hydride in mineral oil and 450 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 oil. Crystallization from ether gave off-white crystals. A small portion was recrystallized from a mixture of methylene chloride and ether to give colorless prisms, mp 201°-202°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04428878 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-2c719291cf444e0f8c0f363ea6c61730 |
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| Source note | uspto-grants-1984_01 |
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