Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440704Generated: October 30, 2026

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

https://huagongshe.com/reaction/440704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1,1-Dimethylethyl (((2,4,6-trimethylphenyl)sulphonyl)oxy)carbamateHCID 359285—
ProductO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 118308450.1%

Reaction Steps

Trifluoroacetic acid, 80.0 mL, was stirred and cooled in an ice-water bath, and 25.0 grams (0,079 mole) of 1,1-dimethylethyl N-(2,4,6-trimethylphenylsulfonyloxy)carbamate was added portionwise. Upon completion of the addition, the reaction mixture was stirred for 90 minutes, then poured into ice-water The resultant solid was collected by filtration and dissolved in diethyl ether. The solution was then dried with magnesium sulfate and filtered. The solid product was precipitated from the filtrate by the addition of petroleum ether. The solid was collected by filtration, yielding 14.4 grams of 1-aminooxysulfonyl-2,4,6-trimethylbenzene. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521147
Source datasetuspto-grants-1996_05
ORD IDord-1a7954263c39476bb49742ebb194580a
Source noteuspto-grants-1996_05