HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Tert-butyl 4-(hydroxymethyl)-4-(methoxymethyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | 1-Tert-butyl 4-ethyl 4-(methoxymethyl)piperidine-1,4-dicarboxylate | HCID 66741448 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl 4-(hydroxymethyl)-4-(methoxymethyl)piperidine-1-carboxylate | HCID 68533155 | 53.9% |
Reaction Steps
To a solution of 1-tert-butyl 4-ethyl 4-(methoxymethyl)piperidine-1,4-dicarboxylate (2.05 g) in toluene (21 ml) was added 0.99 M solution of diisobutyl aluminum hydride in toluene (16.5 ml) under at 0° C. It was stirred at room temperature for 2 hours. Water was added and extracted with EtOAc. The organic phase was washed with water and brine, dried over MgSO4, evaporated off. The residue was purified by silica gel column to give tert-butyl 4-(hydroxymethyl)-4-(methoxymethyl)piperidine-1-carboxylate (0.95 g) as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08603975B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-2797af7e864445298a079f5b512c8fbf |
| Source note | uspto-grants-2013_12 |