HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → 5-t-butyl-2-methoxy-3-nitrophenyl N-t-butyl sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | HCID 15029584 | HCID 15029584 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-t-butyl-2-methoxy-3-nitrophenyl N-t-butyl sulfonamide | HCID 15029585 | — |
Reaction Steps
t-Butylamine (9 ml) was added to a cooled solution of 5-t-butyl-2-methoxy-3-nitrophenyl sulfonyl chloride (7.4 g) in acetonitrile (40 ml). The mixture was stirred at ambient temperature for 1 hour and then the solvent was removed under vacuum. The residue was shaken with ethyl acetate (100 ml) and 4% citric acid (100 ml). The organic phase was separated and dried over sodium sulphate. Evaporation of solvent gave a solid residue which was recrystallized from aqueous ethanol to give the title compound (6.0 g);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04929269 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-9628ff5013cb4231a66d02b35c6cd874 |
| Source note | uspto-grants-1990_05 |