HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → N-tert-Butyl 4-Nitrophenylsulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 4-Nitrobenzenesulfonyl chloride | HCID 7404 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-tert-Butyl 4-Nitrophenylsulfonamide | HCID 796974 | 97% |
Reaction Steps
To a solution of tert-butylamine (0.47 L, 6.4 mol) in THF (0.55 L) is slowly added, at 0° C., a solution of 4-nitrobenzenesulfonyl chloride (50 g, 0.23 mol) in THF (0.55 L) and the resulting mixture is stirred for 24 h at room temperature. The solvent is removed and the residue is taken up in a CHCl3/0.5 N HCl mixture, the layers are separated and the aqueous phase is extracted with CHCl3. The combined organic extracts are washed with H2O and brine and dried over MgSO4. The solvent is removed, yielding 56.3 g of a yellowish solid which is directly used in the next reaction (yield: 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351836B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-8e0bf814a36c4acdbd953b764e2b515b |
| Source note | uspto-grants-2008_04 |