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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593262Generated: November 1, 2026

4-Methoxy-2-nitroaniline → 2-(4-(4-Methoxy-2-nitrophenylaminosulfonyl)phenoxy)acetamide

https://huagongshe.com/reaction/1593262

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-2-nitroanilineHCID 66793—
Reactant4-(2-Amino-2-oxoethoxy)benzenesulfonyl chlorideHCID 11644496—
SolventPyridineHCID 1049—
Product2-(4-(4-Methoxy-2-nitrophenylaminosulfonyl)phenoxy)acetamideHCID 1171786668%

Reaction Steps

Solid 2-[4-(chlorosulfonyl)phenoxy]acetamide (Intermediate A91, 65.87 g, 0.264 mol) was added to a solution of 4-methoxy-2-nitroaniline (27.72 g, 0.165 mol) in pyridine (500 mL) at room temperature under argon. The resulting mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure. To the residue was added 0.5 M hydrochloric acid (1000 mL) and stirred for 30 min. The orange solid was collected and recrystallized from acetone to give 42.8 g (68%) of the title compound, nitro sulfonamide as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294716B2
Source datasetuspto-grants-2007_11
ORD IDord-2c5c5e722d2d4a8a989ae8a9272059c2
Source noteuspto-grants-2007_11