HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 6-Chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine | HCID 10198105 | — |
| Product | 4-Acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine | HCID 9837680 | — |
Reaction Steps
A solution of 6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine (1.6 g, prepared in a similar manner to its hydrochloride, Example 1 above) in acetic anhydride (15 ml) was stirred at room temperature for one hour. The reaction mixture was poured into ice and extracted with dichloromethane. The organic layer was dried and the solvent was removed by evaporation to give 4-acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine, which was recrystallised from hexane. Yield 1.68 g (m.p. 79°-81° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05580866 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-301c65891e2b48c9899050c466b29565 |
| Source note | uspto-grants-1996_12 |