Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | HCID 23712331 | HCID 23712331 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20471873 | HCID 20471873 | 61.5% |
Reaction Steps
At a temperature of 30° to 50° C., 248 gm (1.35 mol) of sodium 5-methyl-furan-2-sulfonate were admixed in portions with 281 gm (1.35 mol) of phosphorus pentachloride and the mixture was stirred for 15 minutes at 50° C. The reaction mixture was then poured over ice and extracted with ether. The ether phase was washed until neutral, dried and evaporated. The residue (200 gm of 5-methyl-furan-2-sulfonic acid chloride) was dissolved in 500 ml of ether, and the solution was added dropwise to a solution of 280 ml (2.7 mol) of tert.-butylamine in 500 ml of ether at a temperature of 5° to 10° C. After stirring at room temperature and at reflux temperature, each for 2 hours, the reaction mixture was washed with ice water, dilute hydrochloric acid and water and then evaporated. The residue was recrystallized from cyclohexane, yielding 180.5 gm (61.5L % of theory) of N-tert.-butyl-5-methyl-furan- 2-sulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04430355 |
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| Source dataset | uspto-grants-1984_02 |
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| ORD ID | ord-5a8c08aae84c463987bb92ad47dba4c0 |
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| Source note | uspto-grants-1984_02 |
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