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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-tert-Butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamideHCID 19693794—
SolventChloroformHCID 6212—
ProductN-tert-Butyl-2-methoxycarbonyl-5-methylaminobenzenesulfonamideHCID 19693799—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05449812
Source datasetuspto-grants-1995_09
ORD IDord-cfae78fceb714553a0b7edce08385c9b
Source noteuspto-grants-1995_09