HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2-Dioxo-6-(1,1-dimethylethyl)-8-chloro-1,2,3-benzoxathiazine → HCID 23342885, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2-Dioxo-6-(1,1-dimethylethyl)-8-chloro-1,2,3-benzoxathiazine | HCID 23342889 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 23342885 | HCID 23342885 | 93% |
Reaction Steps
A solution of 2,2-dioxo-6-(1,1-dimethylethyl)-8-chloro-1,2,3-benzoxathiazine (2.5 g., 9.2 millimole) in acetic acid (200 ml.) contained in a Parr apparatus is hydrogenated in the presence of platinum (IV) oxide at 20° C. and a pressure (initial) of 50 p.s.i. for five minutes. The catalyst is removed by filtration and the filtrate is evaporated in vocuo to provide the title compound as a residual solid (2.35 g., 93%), m.p. 158°-160° C. Crystallization from 50% ethanol gives analytically pure 2,2-dioxo-3,4-dihydro-6-(1,1-dimethylethyl)-8-chloro-1,2,3-benzoxathiazine as colorless crystals, m.p. 162°-163° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04166177 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-1cae3cc411f34bd28626a327194fd315 |
| Source note | uspto-grants-1979_08 |