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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 998Generated: October 25, 2026

Formic Acid → N-tert-Butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamide

https://huagongshe.com/reaction/998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAcetic AnhydrideHCID 7918—
Reactantmethyl 4-amino-2-(N-tert-butylsulfamoyl)benzoateHCID 10946074—
SolventDimethylformamideHCID 6228—
ProductN-tert-Butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamideHCID 19693794—

Reaction Steps

6.5 ml of formic acid are carefully added at 0° C. to 13 ml of acetic anhydride. The mixture is subsequently heated at 50°-60° C. for 2 h. A solution of 16.0 g (0.056 mol) of N-tert-butyl-5-amino-2-methoxycarbonylbenzenesulfonamide in 50 ml of DMF is then added dropwise at 0° C. The cooling bath is removed and the mixture is stirred for a further 4 h at room temperature. The reaction mixture is then shaken up in 800 ml of ethyl acetate and washed with three times 150 ml of water. The organic phase is dried over magnesium sulfate, the solvent is distilled off, and the residue is recrystallized from ethyl acetate/n-heptane. The product is N-tert-butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamide (14.23 g, 82% of theory) which melts at 113°-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723409
Source datasetuspto-grants-1998_03
ORD IDord-e6119d1ed5fd4cad8ff5deeb55d6be7b
Source noteuspto-grants-1998_03