HuagongsheHuagongshe Chemistry Print Report · For research reference only
[2,2'-Bithiophene]-5-carboxaldehyde → (5-Thiophen-2-ylthiophen-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | [2,2'-Bithiophene]-5-carboxaldehyde | HCID 364428 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (5-Thiophen-2-ylthiophen-2-yl)methanol | HCID 2776422 | 99.5% |
Reaction Steps
To a solution of 5-formyl-2,2'-bithiophene (20 g) in methanol (50 ml) was added sodium borohydride. The reaction mixture was stirred at room temperature and monitored with thin layer chromatography until the reaction completed. After removal of methanol, water was added to dissolve inorganic salts and extracted with dichloromethane. The extract was washed with brine, dried over anhydrous magnesium sulfate, concentrated to give product (20.1 g, 99%), melting point 52°-53° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05578636 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-0ff0c8b9995e4d7dad558fc0fcb7e416 |
| Source note | uspto-grants-1996_11 |