Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 57637614 | HCID 57637614 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57637965 | HCID 57637965 | — |
Reaction Steps
To a slurry of LiAlH4 (4 equivalents) in dry THF, cooled to 0° C. under N2, was slowly added drop-wise a solution of methyl 4-[4-(1-BOC-piperazin-4-yl)phenoxymethyl]benzoate (1 equivalent) in dry THF. Once the addition was complete, the slurry was heated to reflux at 80° C. for 1 hour. The slurry was subsequently cooled to 0° C. and treated with water, 10% aq. NaOH and with water again. The resulting solids were filtered, and the filtrate was diluted with chloroform, washed with brine, dried over MgSO4 and concentrated, providing the crude 4-[4-(4-methylpiperazin-1-yl)phenoxymethyl]benzyl alcohol that was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893096B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-7f02eab642c04712b6e415467de8cd7a |
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| Source note | uspto-grants-2011_02 |
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