HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Acetyl-4-hydroxy-1lambda~6~-naphtho[2,1-e][1,2]thiazine-1,1(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-(2-Oxopropyl)-1H-1lambda~6~-naphtho[2,1-d][1,2]thiazole-1,1,3(2H)-trione | HCID 12422731 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Acetyl-4-hydroxy-1lambda~6~-naphtho[2,1-e][1,2]thiazine-1,1(2H)-dione | HCID 12422732 | 54% |
Reaction Steps
28.9 gm (1.0 mol) of 2-acetonyl-3-oxo-naphth[2,1-d]isothiazoline-1,1-dioxide were added to a solution of 4.7 gm (2.04 gm-atom) of sodium in 125 ml of ethanol at 30° C. The resulting mixture was kept at 55° C for 2 hours, while stirring, and was subsequently refluxed for 15 minutes. After cooling, the reaction mixture was acidified with 350 ml of aqueous 9% hydrochloric acid, and the solid product formed thereby was suction-filtered off and washed with ice-cold 50% ethanol. Recrystallization from ethanol yielded 15.6 gm (54% of theory) of 3-acetyl-4-hydroxy-2H-naphtho[2,1-e]-1,2-thiazine-1,1-dioxide, m.p. 191°-192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03992535 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-0f50fbf3eeab4e39b73763392defeae6 |
| Source note | uspto-grants-1976_11 |