HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396899Generated: October 29, 2026
Dichloromethane → N,N-dimethyl-N'-(4-ethyl-2,4-hexadien-1-yl)sulfamide
https://huagongshe.com/reaction/2396899
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Dimethylsulphamoyl chloride | HCID 83372 | — |
| Reactant | 4-Ethyl-2,4-hexadien-1-ylamine | HCID 53945213 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N,N-dimethyl-N'-(4-ethyl-2,4-hexadien-1-yl)sulfamide | HCID 54361333 | — |
Reaction Steps
A mixture of N-(4-ethyl-2,4-hexadien-1-yl)phthalimide (3.0 g), hydrazine monohydrate (0.88 g), and ethanol (30 ml) was refluxed for 40 minutes under nitrogen atmosphere. After cooling, the precipitate was filtered and washed with ethanol. Evaporation of the filtrate gave a crystalline residue which was dissolved in 1N sodium hydroxide solution and extracted with dichloromethane. The organic extract was washed with water and brine, dried over anhydrous sodium sulfate, and evaporated to give 4-ethyl-2,4-hexadien-1-ylamine as an oil. To a mixture of crude 4-ethyl-2,4-hexadien-1-ylamine, triethylamine (1.79 g), and dichloromethane (30 ml) at 0° C. was added dropwise dimethylsulfamoyl chloride (2.03 g) during 10 minutes. After 30 minutes, triethylamine (0.6 g) and dimethylsulfamoyl chloride (0.85 g) were added to the reaction mixture. After 1 hour at 0° C., the reaction mixture was washed with water and aqueous sodium hydrogen carbonate solution, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel (dichloromethane-hexane, 7:3) to give N,N-dimethyl-N'-(4-ethyl-2,4-hexadien-1-yl)sulfamide (924 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05495023 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-f59d88d4e48b45f1bcff587c246b332b |
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| Source note | uspto-grants-1996_02 |
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