HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939854Generated: October 26, 2026
Hydrochloric Acid → N-(4,4-diethoxybutyl)methanesulfonamide
https://huagongshe.com/reaction/1939854
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4,4-Diethoxybutylamine | HCID 80672 | — |
| Reactant | Methane sulfochloride | HCID 19821184 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(4,4-diethoxybutyl)methanesulfonamide | HCID 85717959 | 88% |
Reaction Steps
48.2 g 4-amino butyraldehyde diethyl acetal are dissolved in 48.2 g water-free pyridine at 20 ° C. under stirring in a three-necked flask, equipped with a thermometer, reflux condenser, tap funnel and magnetic stirrer. Subsequently, the mixture is cooled to 10° to 15° C. by means of external cooling and at these temperatures 34,6 g methane sulfochloride is added drop-wise at such a rate that the temperature of the reaction mixture does not rise beyond the given range. Subsequently, the mixture is heated to 40° to 50° C. for 1 hour and then stirred into 300 g ice water, to which 20 g of concentrated hydrochloric acid were added, under intensive stirring. The resulting substance is a two-phase, yellow-brown mixture, which is extracted with ether and further processed as explained in Preparation Example 1. Yield: 88% based on the amino acetal used.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05698360 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-13753f911c5b4a8eb3aeeb2cfa03da01 |
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| Source note | uspto-grants-1997_12 |
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