HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl formate → 1-Boc-4-[(1-methyl-4-piperidyl)methyl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 4-Piperidin-4-ylmethyl-piperidine-1-carboxylic acid t-butyl ester | HCID 49761197 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Boc-4-[(1-methyl-4-piperidyl)methyl]piperidine | HCID 68888922 | — |
Reaction Steps
1,1-Dimethylethyl 4-(4-piperidinylmethyl)-1-piperidinecarboxylate (may be prepared as described in Description 2) (1.5 g), and LiAlH4 (26.6 ml of 1M solution in tetrahydrofuran) were combined in tetrahydrofuran (10 ml) and the reaction mixture stirred at room temperature for 10 min before cooling to 0° C. in an ice/water bath. Ethyl formate (5 ml) was then added dropwise. The reaction was then quenched with 3 N sodium hydroxide solution. The solid precipitate formed was filtered and washed with more tetrahydrofuran. The combined organics were dried over Na2SO4, and evaporated to give the title compound (D18) (1.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07638631B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-7cdeab6b0ba04e769d77c58f584344a8 |
| Source note | uspto-grants-2009_12 |