HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399587Generated: October 27, 2026
Methanol → N-tert-Butyl-2-methoxycarbonyl-5-methylaminobenzenesulfonamide
https://huagongshe.com/reaction/2399587
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | N-tert-Butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamide | HCID 19693794 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-tert-Butyl-2-methoxycarbonyl-5-methylaminobenzenesulfonamide | HCID 19693799 | — |
Reaction Steps
9.92 g (0.032 mol) of N-tert-butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamide are dissolved in 50 ml of CHCl3, and then 5 ml (0.053 mol) of boranedimethyl sulfide complex are added at 0° C. After 1 h at 0° C. and 3 h at room temperature the reaction mixture is cooled to 0° C. 30 ml of methanol are added and the mixture is washed with water. The organic phase is dried over magnesium sulfate, the solvent is removed by distillation, and 9.23 g (98% of theory) of N-tert-butyl-2-methoxycarbonyl-5-methylaminobenzenesulfonamide are obtained. m.p.: 120°-124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05449812 |
|---|
| Source dataset | uspto-grants-1995_09 |
|---|
| ORD ID | ord-cfae78fceb714553a0b7edce08385c9b |
|---|
| Source note | uspto-grants-1995_09 |
|---|