HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → 6,7-Dichloro-5-hydroxy-2-hydroxymethylbenzo[b]thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6,7-Dichloro-2-formyl-5-hydroxybenzo[b]thiophene | HCID 13290037 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6,7-Dichloro-5-hydroxy-2-hydroxymethylbenzo[b]thiophene | HCID 13290038 | 74.4% |
Reaction Steps
To a solution of 6.0 g of 6,7-dichloro-2-formyl-5-hydroxybenzo[b]thiophene and 300 ml of 90% ethanol is added portionwise 1.5 g of sodium borohydride. The reaction mixture is stirred at room temperature for 20 min. Saturated sodium chloride solution is added and the mixture is extracted three times with ethyl acetate:ether (1:1). The combined organic extracts are washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate and evaporated to give 4.5 g of 6,7-dichloro-5-hydroxy-2-hydroxymethylbenzo[b]thiophene, mp 167°-169°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04672138 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-446f0d206f0d48bab133e3420746b254 |
| Source note | uspto-grants-1987_06 |