HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cornforth reagent → (S)-1-(2-thiopheneacetyl)-3-piperidinecarboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cornforth reagent | HCID 2724130 | — |
| Reactant | (S)-ethyl 1-(2-thiopheneacetyl)-3-hydroxymethylpiperidine | HCID 86759306 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-1-(2-thiopheneacetyl)-3-piperidinecarboxaldehyde | HCID 28271707 | 32.6% |
Reaction Steps
(S)-ethyl 1-(2-thiopheneacetyl)-3-hydroxymethylpiperidine (180.4 ml; 0.75 mmol) was dissolved in dichloromethane (20 ml). Crushed molecular sieves (0.25 g), and commercially available pyridinium dichromate (331.2 mg; 0.88 mmol) were added and the mixture was allowed to stir at ambient temperature for 5 hours. The mixture was then filtered through celite, washed with decolorizing carbon, filtered again and then evaporated under reduced pressure at ambient temperature. Crude product was purified by distillation at approximately 250° C./0.1 torr, giving (S)-1-(2-thiopheneacetyl)-3-piperidinecarboxaldehyde (58 mg) as a thick colorless oil. MS m/z (positive ion) 317 (25), 238 (MH+; 100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06664271B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-371169213b284b818385f33124448ed9 |
| Source note | uspto-grants-2003_12 |