Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfur DioxideHCID 1119—
Reactant2-Amino-N,N-diethylbenzenesulfonamideHCID 12819598—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductN,N-diethyl-1,2-benzenedisulfonamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04342587
Source datasetuspto-grants-1982_08
ORD IDord-33bf67604ebc4e2f9cdc40e3a2235270
Source noteuspto-grants-1982_08