HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 4-Acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 4-Acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine | HCID 9837680 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxide | HCID 10220764 | — |
Reaction Steps
A solution of 3-chloroperbenzoic acid (1.14 g) in dichloromethane (100 ml) was added dropwise with cooling from 0° C. to -2° C. to a stirred solution of 4-acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine (1.34 g, prepared as Example 9 above) in dichloromethane (50 ml). The reaction mixture was stirred for 15 minutes, washed with water, dried and the solvent was removed by evaporation at reduced pressure. Purification of the residue by flash chromatography using dichloromethane/ethanol (95:5) as eluent gave 4-acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxide, which was recrystallised from ethyl acetate. Yield 1.15 g (m.p. 119°-121° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05580866 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-3c268fbe2ed54558a799f9b25e0286dd |
| Source note | uspto-grants-1996_12 |