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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717548Generated: October 29, 2026

Trifluoroacetic acid → O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamine

https://huagongshe.com/reaction/717548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1,1-Dimethylethyl (((2,4,6-trimethylphenyl)sulphonyl)oxy)carbamateHCID 359285—
ProductO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193724B2
Source datasetuspto-grants-2015_11
ORD IDord-5ceeb858816c4bb6824b68e03e1b5ae3
Source noteuspto-grants-2015_11