HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → N-(1,1-Dimethylethyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1,1-Dimethylethyl)benzenesulfonamide | HCID 314059 | — |
Reaction Steps
To a solution of benzenesulfonyl chloride in anhydrous CH2Cl2 (0.5M solution) cooled to 0° C. under N2 was added t-butylamine (2.2 equiv) slowly through a dropping funnel. After completion of addition, the reaction was stirred at toom temperature for 12 hours. The solvent was removed under reduced pressure, and the residue was extracted into ether and washed with 2N NaOH, H2O and brine. The organic phase was dried over anhydrous MgSO4 and concentrated in vacuo to afford the titled product, which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05436259 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-b80ef7096ed543a8bea75956d2d5491f |
| Source note | uspto-grants-1995_07 |