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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1,1-Dimethylethyl (((2,4,6-trimethylphenyl)sulphonyl)oxy)carbamate | HCID 359285 | — |
| Solvent | Water | HCID 962 | — |
| Product | O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamine | HCID 11830845 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09173887B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-a9232f0a74524116b766985a1d21d841 |
|---|
| Source note | uspto-grants-2015_11 |
|---|