HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 66670254, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86626939 | HCID 86626939 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66670254 | HCID 66670254 | — |
Reaction Steps
A 750 mg portion of ethyl 5-tert-butyl-1-[2-(4-fluorophenyl)ethyl]-4-formyl-2-methyl-1H-pyrrole-3-carboxylate was suspended in 15 ml of ethanol, and 158 mg of sodium borohydride was added at 0° C., followed by stirring at room temperature for 2 hours. The solvent was evaporated under a reduced pressure, chloroform and water were added, and the organic layer was washed with saturated brine and then dried over anhydrous sodium sulfate. By evaporating the solvent under a reduced pressure, 754 mg of ethyl 5-tert-butyl-1-[2-(4-fluorophenyl)ethyl]-4-(hydroxymethyl)-2-methyl-1H-pyrrole-3-carboxylate was obtained as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08222274B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-0f893527366c4cc5b5a3167ff25c4499 |
| Source note | uspto-grants-2012_07 |