HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Piperidinecarboxaldehyde → HCID 15017674, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Piperidinecarboxaldehyde | HCID 17429 | — |
| Reactant | 1-Bromo-2,4,5-trifluorobenzene | HCID 67597 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15017674 | HCID 15017674 | 45.3% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a solution of 1-bromo-2,4,5-trifluoro benzene (25 g, 0.12 mol) in THF (200 mL at -78° C. was added LDA (80 mL, 1.5 M) dropwise. The mixture was stirred at -78° C. for 1 hour, then N-formylpiperidine (16 g, 0.144 mol) was added in one portion and stirring continued for 2 hours. An additional 15 g of N-formylpiperidine was then added every 0.5 hour in 5 g portions. The reaction was quenched with 3N HCl (pH 3) at -78° C. The reaction was warmed to 0° C. and partitioned between H2O and ether. The ether layer was dried and concentrated and the residue was distilled to provide 13 g (45%) of the desired aldehyde; bp 63°-65° C. (0.2 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05116834 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-84f19543d27e4a6f986004fbe8991e49 |
| Source note | uspto-grants-1992_05 |