HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1,1-Dimethylethyl (((2,4,6-trimethylphenyl)sulphonyl)oxy)carbamate | HCID 359285 | — |
| Product | O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamine | HCID 11830845 | — |
Reaction Steps
Trifluoroacetic acid (20 mL) was cooled to 0° C., then tert-butyl(mesitylsulfonyl)oxycarbamate (J; 6 g, 0.0189 mol) was added portion wise for 30 min. The reaction mixture was allowed to stir for 2 h at the same temperature. Ice cold water (150 mL) was added and the reaction mixture was stirred for 15 min to form a precipitate, which was filtered to get a solid compound. The solid was dried under vacuum to afford 2-[(aminooxy)sulfonyl]-1,3,5-trimethylbenzene. 1H NMR (400 MHz, CDCl3) δ 8.62 (s, 1H), 8.56 (s, 1H), 2.56 (s, 3H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193724B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-5ceeb858816c4bb6824b68e03e1b5ae3 |
| Source note | uspto-grants-2015_11 |