HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium bisulfate → tert-Butyl 4-formylpiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | tert-Butyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate | HCID 11065582 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 4-formylpiperidine-1-carboxylate | HCID 1514430 | 108% |
Reaction Steps
A solution of 5.46 g (143.8 mmol) of LAH in 600 ml THF was cooled (−50° C.) and treated during 25 min with a solution of 35.6 g (130.7 mmol) of 4-(Methoxy-methyl-carbamoyl)-piperidine-1-carboxylic acid tert-butyl ester in 600 ml THF. The reaction was warmed up to RT for 3.5 h, cooled (−78° C.) and hydrolyzed with a suspension of 35 g MgSO4.7H2O, 35 g silicagel in 130 ml aqueous 10% KHSO4. The cooling bath was removed, THF was added, the mixture was stirred for 30 min and filtered. After evaporation, the residue was dissolved in CH2Cl2, dried (Na2SO4) and evaporated to give 30.1 g (quantitative) of 4-Formyl-piperidine-1-carboxylic acid tert-butyl ester, MS: 213 (M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06964974B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-f4fd6cf886844fe1ba60134930b60649 |
| Source note | uspto-grants-2005_11 |