Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 23153146 | HCID 23153146 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23153447 | HCID 23153447 | 104.3% |
Reaction Steps
A suspension of lithium aluminum hydride (405 mg) in tetrahydrofuran (10 ml) was stirred while cooling in an ice water bath under a nitrogen atmosphere. 1-(Azetidin-1-yl)-2-(4-benzoylpiperazin-1-yl)ethanone (730 mg) and tetrahydrofuran (5 ml×3) were added thereto. The reaction mixture was stirred at 60° C. for 3 hrs. The reaction mixture was then cooled to room temperature. Water (0.40 ml), 5N aqueous sodium hydroxide (0.40 ml) and water (1.2 ml) were added thereto, and the reaction mixture was stirred for 13 hrs. The reaction mixture was passed through Celite to remove the insoluble material. The insoluble material was washed with ethyl acetate (100 ml). The solvent was evaporated to provide a crude product of the titled compound (687 mg) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531532B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-e6c2702a3a284736aab17eee3e21ed3e |
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| Source note | uspto-grants-2009_05 |
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