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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395635Generated: October 31, 2026

Triethylamine → HCID 86736898, compound

https://huagongshe.com/reaction/1395635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzenesulfonyl fluoride, 3-(chlorosulfonyl)-HCID 75603—
ReactantHCID 20448267HCID 20448267—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86736898HCID 86736898166.2%

Reaction Conditions

Temperature5 °C

Reaction Steps

2'-Amino-4'-nitromethanesulfonanilide (30.4 g; 0.13 mole) was dissolved in dry tetrahydrofuran (ca. 700 ml) and then triethylamine (13.1 g; 0.13 mole) was added and the solution was chilled to 5° C. While stirring and maintaining a temperature <10° C., While stirring and maintaining a temperature <10° C., m-fluorosulfonylbenzenesulfonyl chloride (33.8 g; 0.13 mole) was added dropwise. After the addition, the reaction was kept at the ice bath temperature for one hour and then stirring continued at room temperature for an additional hour. The reaction solution was poured into ice cold water (about 2 liters) while stirring and scratching vigorously. The product was filtered and dried to yield 50.6 g (85 percent) beige solid, m.p. 204° to 209° C. A small sample (1 g) was recrystallized from ethanol (150 ml) to yield a beige solid, m.p. 224° to 226° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04204993
Source datasetuspto-grants-1980_05
ORD IDord-dd262aabefff404ba0fb38bed0af86c7
Source noteuspto-grants-1980_05