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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705364Generated: October 31, 2026

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

https://huagongshe.com/reaction/705364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1,1-Dimethylethyl (((2,4,6-trimethylphenyl)sulphonyl)oxy)carbamateHCID 359285—
SolventWaterHCID 962—
ProductO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyl mesitylsulfonyloxycarbamate (1.51 g, 5.42 mmol) was added to cold (0° C.) trifluoroacetic acid (10.8 mL) and the mixture was stirred at 0° C. for 45 minutes. The mixture was diluted with cold (0° C.) water and the white precipitate was collected by filtration and washed with 1000 mL of cold (0° C.) water. The solid was dried by suction for about 5 minutes and then dissolved in cold (0° C.) dichloromethane and dried (Na2SO4). The solution was filtered and the filtrate was concentrated to a volume of about 12 mL on the rotary evaporator without heating. The solution was then directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173887B2
Source datasetuspto-grants-2015_11
ORD IDord-a9232f0a74524116b766985a1d21d841
Source noteuspto-grants-2015_11