HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 7-Methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18921799 | HCID 18921799 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine | HCID 14548169 | 97.2% |
Reaction Steps
Sodium borohydride(4.4 g, 116 mmol) was added portionwise at room temperature to a mixture solution of 7-methyl-6,7-dihydrothieno[2,3-c]pyridine(10.5 g, 69.4 mmol) prepared in the above Step 2 and ethanol(100 ml). After stirring for 1 hour, the reaction mixture was diluted with water, and extracted with dichloromethane. The combined dichloromethane layers were dried over magnesium sulfate and concentrated to give 10.34 g of the titled compound. (Yield: 97%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05750531 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-c9cf938a6fb744f08f9ed50bda957f82 |
| Source note | uspto-grants-1998_05 |