HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Chloride → 3-Hydroxylmethyl-benzoylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Ethoxycarbonyl-benzoylpiperazine | HCID 54361860 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Hydroxylmethyl-benzoylpiperazine | HCID 18519751 | — |
Reaction Steps
To a stirred solution of 3-ethoxycarbonyl-benzoylpiperazine XLIX (200 mg, 0.76 mmol) in THF (5 ml), was added lithium chloride (36 mg, 0.84 mmol), NaBH4 (32 mg, 0.84 mmol) and EtOH (5 ml) sequentially. After stirring for 8 hours at room temperature, a saturated NaHCO3 solution was added and the aqueous phase was extracted with ethyl acetate (3×20 ml). The organic layers were combined, dried over MgSO4 and concentrated to give a crude mixture, which was used for the further reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06469006B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-858d69991262437685df9be6dd8a01e8 |
| Source note | uspto-grants-2002_10 |