HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → Tert-butyl 4-[3-(hydroxymethyl)phenyl]piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | 1-Boc-4-(3-(ethoxycarbonyl)phenyl)piperazine | HCID 16217941 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-[3-(hydroxymethyl)phenyl]piperazine-1-carboxylate | HCID 29949342 | 90% |
Reaction Steps
tert-Butyl-4-(3-(ethoxycarbonyl)phenyl)piperazine-1-carboxylate (0.20 g, 0.60 mmol) was dissolved in THF (1 mL) and lithium borohydride (0.10 g, 7.5 eq) was added in three portions. The reaction mixture stirred at rt for 48 h then quenched with saturated ammonium chloride under ice-cooling. The aqueous phase was extracted with DCM and the combined organic phases dried over sodium sulfate and evaporated to afford tert-butyl 4-(3-(hydroxymethyl)phenyl)piperazine-1-carboxylate (0.16 mg, 0.54 mmol, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040545B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-bb90e575d8874a27b8e5373e94d6bc73 |
| Source note | uspto-grants-2015_05 |