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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | methyl 4-amino-2-(N-tert-butylsulfamoyl)benzoate | HCID 10946074 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-tert-Butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05723409 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-e6119d1ed5fd4cad8ff5deeb55d6be7b |
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| Source note | uspto-grants-1998_03 |
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