HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613769Generated: October 31, 2026
Triethylamine → Sulfamic acid 4-oxo-4-phenylbutyl ester
https://huagongshe.com/reaction/1613769
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosulfamic acid | HCID 24499 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 4-Hydroxy-1-phenylbutan-1-one | HCID 10975816 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Sulfamic acid 4-oxo-4-phenylbutyl ester | HCID 54177453 | 40.1% |
Reaction Steps
A cold (-10° C.) solution of 5.20 ml (0.06 mole) chlorosulfonyl isocyanate in 50 ml of methylene chloride was treated with a solution of 0.11 ml of water in 5 ml of acetonitrile over a period of 30 min. A solution of 6.56 g (0.04 mole) of 4-oxo-4-phenylbutanol and 8.34 ml (0.06 mole) of triethylamine in 30 ml of methylene chloride was then added to the solution of the sulfamoyl chloride at 0° to 10° C. over 20 min. The reaction mixture was stirred at room temperature for 4 hr. extracted once with water and once with sodium bicarbonate solution. The aqueous layers were back extracted with methylene chloride. The combined organic layers were dried (magnesium sulfate) and concentrated to an oil that solidified on standing. The solid was triturated with 1,1,1-trichloroethane to give 3.90 g of off-white solid. Recrystallization from acetonitrile-1,1,1-trichloroethane yielded 3.2 g of off-white solid, mp 78°-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05194446 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-1fedc2e8be684cc189e85348f48cf0a6 |
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| Source note | uspto-grants-1993_03 |
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