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 | — |
Reaction Steps
20 g of 5-formyl-2,2'-bithiophene was dissolved in 50 ml of methanol, followed by adding NaBH4 and stirring until bubbling stopped. The reaction was monitored by thin layer chromatography to determine whether the reaction was completed. After the methanol was removed under reduced pressure and the reaction solution was extracted with dichloromethane, the solution was washed with saturated NaCl solution, dried over anhydrous magnesium sulfate, condensed and 20.10 g of product (melting point 52°-53° C., 99%) was thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05602170 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-b4a3337ae51f48bba59e37017ca88289 |
| Source note | uspto-grants-1997_02 |