HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (+/-)-2,7-Dichloro-4H-benzo[5,6]cyclohepta[1,2-d]thiazol-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,7-Dichloro-4H-benzo[5,6]cyclohepta[1,2-d]thiazol-4-one | HCID 22003621 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (+/-)-2,7-Dichloro-4H-benzo[5,6]cyclohepta[1,2-d]thiazol-4-ol | HCID 70113755 | — |
Reaction Steps
Sodium borohydride (0.159 g) was added to a suspension of the product from step (vi) (1.27 g) in methanol (20 ml) and dichloromethane (5 ml) at room temperature. After 3 h the mixture was partitioned between 2N NaOH and dichloromethane. The organic phase was collected, dried, (MgSO4) and solvent evaporated to leave a colourless foam. Yield: 1.27 g Used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218376B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-3730e788ac444b46a21c70c556d18e6f |
| Source note | uspto-grants-2001_04 |