HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 13952868, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20197895 | HCID 20197895 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13952868 | HCID 13952868 | — |
Reaction Steps
Sodium borohydride (2.5 g) is added, in small portions, to a stirred solution of 5.0 g of 6,7-dichloro-5-methoxy-2-methylbenzo[b]thiophen-3(2H)-one (5.0 g), in 120 ml of ethanol. Stirring is continued at room temperature for 1 hour and excess solvent is removed under reduced pressure. The residue is triturated with dilute sodium hydroxide solution and extracted 3 times with ether. The combined ether solution is washed thoroughly with water, dried and concentrated. Removal of ether leaves an oily residue which crystallized upon cooling. For analysis, a small sample was washed with pentane and dried at 60° C. to give 6,7-dichloro-2,3-dihydro-3-hydroxy-5-methoxy-2-methylbenzo[b]thiophene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04537976 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-cca494339e3a435ba7ac9e1eb82b22cb |
| Source note | uspto-grants-1985_08 |