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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300971Generated: October 29, 2026

Tert-Butylamine → methyl 2-(N-tert-butylsulfamoyl)-4-nitrobenzoate

https://huagongshe.com/reaction/2300971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantMethyl 2-(chlorosulfonyl)-4-nitrobenzoateHCID 15240541—
SolventEthyl AcetateHCID 8857—
Productmethyl 2-(N-tert-butylsulfamoyl)-4-nitrobenzoateHCID 15240542—

Reaction Steps

206 g of tert-butylamine are added dropwise to a solution of 384 g of methyl 2-chlorosulfonyl-4-nitro-benzoate (Example b) in 1500 ml of ethyl acetate at 0° C. The reaction mixture is then allowed to warm up to room temperature and is stirred at this temperature for 1 hour. After washing with dilute hydrochloric acid and water, the organic phase is dried over MgSO4 and concentrated. The residue is extracted by stirring with diisopropyl ether; Yield of sulfonamide: 377.6 g; m.p.: 122-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498253B1
Source datasetuspto-grants-2002_12
ORD IDord-fa067522dd3944488487a7fb25541f81
Source noteuspto-grants-2002_12