HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096254Generated: November 1, 2026
Acetic Acid → 3-[3-Methyl-2-oxo-4-(3-trifluoromethoxy-phenyl)-piperazin-1-yl]-propionaldehyde
https://huagongshe.com/reaction/1096254
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | N-Methoxy-N-methyl-3-[3-methyl-2-oxo-4-(3-trifluoromethoxy-phenyl)-piperazin-1-yl]-propionamide | HCID 86638390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[3-Methyl-2-oxo-4-(3-trifluoromethoxy-phenyl)-piperazin-1-yl]-propionaldehyde | HCID 86638391 | 80.3% |
Reaction Steps
Lithium aluminum hydride solution (1 M in THF (0.46 mL, 0.46 mmol) was added dropwise at −30° C. to a solution of N-methoxy-N-methyl-3-[3-methyl-2-oxo-4-(3-trifluoromethoxy-phenyl)-piperazin-1-yl]-propionamide (180 mg, 0.46 mmol) in THF (10 mL). The reaction mixture was cooled to −75° C., then acetone (0.59 g, 10 mmol) and AcOH (44 mg, 0.93 mmol) were added dropwise. The reaction mixture was then partitioned between TBME and 1 M aq. KHSO4 solution. The organic layer was dried (MgSO4), filtered, and evaporated to afford the title compound (122 mg, 80%). Light yellow oil, MS: 331.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138175B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-78b0ffe61b8a4a5e9faf065a96a35023 |
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| Source note | uspto-grants-2012_03 |
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