HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (S)-tert-butyl 3-(1-hydroxyethyl)pyrrolidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | tert-Butyl (3S)-3-acetylpyrrolidine-1-carboxylate | HCID 68071565 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-tert-butyl 3-(1-hydroxyethyl)pyrrolidine-1-carboxylate | HCID 71113442 | — |
Reaction Steps
To a solution of (S)-tert-butyl 3-acetylpyrrolidine-1-carboxylate in methanol (10 mL) was added sodium borohydride (114 mg, 3.0 mmol) at 0° C. The reaction mixture was stirred at ambient temperature for 2 hours then quenched with saturated ammonium chloride solution and extracted with dichloromethane. The combined extracts were dried over magnesium sulfate, filtered, and concentrated to give the title compound for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434726B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-4fb5d22d6b59418ba567344c09e3fb35 |
| Source note | uspto-grants-2016_09 |