HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66446Generated: October 27, 2026
Sulfur Dioxide → N,N-diethyl-1,2-benzenedisulfonamide
https://huagongshe.com/reaction/66446
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | 2-Amino-N,N-diethylbenzenesulfonamide | HCID 12819598 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | N,N-diethyl-1,2-benzenedisulfonamide | HCID 12819600 | — |
Reaction Steps
To a solution of 114 g of o-amino-N,N-diethylbenzenesulfonamide in a mixture of 400 ml of concentrated hydrochloric acid and 100 ml of glacial acetic acid was added a solution of 50 g of sodium nitrite in 130 ml of water at -5° to 0°. The solution was stirred at 0° for 15 minutes then poured into a mixture of 14 g of cuprous chloride and 100 ml of liquid sulfur dioxide in 550 ml of glacial acetic acid at 0°-5°. This mixture was stirred at 0° for 15 minutes then at room temperature for 3 hours before pouring into three liters of ice water. The crude sulfonyl chloride was filtered off and washed with water. It was then dissolved in 1 l of ethyl ether, washed with water and dried over magnesium sulfate. To this ether solution was added 20 ml of liquid anhydrous ammonia at 5°-15°. After stirring overnight at room temperature the solid was filtered off, washed with water, ethanol and then 1-chlorobutane. Oven drying at 60° gave 91.8 g N,N-diethyl-1,2-benzenedisulfonamide, m.p. 156°-9°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04342587 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-33bf67604ebc4e2f9cdc40e3a2235270 |
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| Source note | uspto-grants-1982_08 |
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