HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22415Generated: October 26, 2026
Phenethylamine → 4-((2-Phenylethyl)aminocarbonyl)benzenesulfonamide
https://huagongshe.com/reaction/22415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Carzenide | HCID 8739 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-((2-Phenylethyl)aminocarbonyl)benzenesulfonamide | HCID 19970748 | 67% |
Reaction Steps
20.1 g (0.1 mol) of 4-carboxy-benzenesulfonamide were suspended in 300 ml of anhydrous tetrahydrofuran, and 15.2 ml (0.11 mol) of triethylamine were added dropwise at 0° C., while stirring. After 30 minutes, 10.5 ml (0.11 mol) of ethyl chloroformate were added dropwise at 0° C., the mixture was stirred at this temperature for 1 hour and cooled to -10° C., and 12.1 g (0.1 mol, 12.5 ml) of 2-phenylethylamine in 30 ml of anhydrous tetrahydrofuran were added dropwise. After 1 hour at 0° C., the mixture was warmed to 20° C. and concentrated in vacuo and the solid residue was treated with water, filtered off with suction and recrystallized from ethanol to give 20.4 g of product, melting point 243° to 245° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05428046 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-350c9a4b7662438bb680d09920db4e0a |
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| Source note | uspto-grants-1995_06 |
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