HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Tert-butyl 1-[2-(benzyloxy)-2-oxoethyl]piperidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl bromoacetate | HCID 62576 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Tert-butyl Piperidine-4-carboxylate | HCID 1512676 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Tert-butyl 1-[2-(benzyloxy)-2-oxoethyl]piperidine-4-carboxylate | HCID 66588152 | — |
Reaction Steps
To a suspension (39 mL) of tert-butyl piperidine-4-carboxylate (2.6 g) in acetonitrile was added diisopropylethylamine (4.4 mL), subsequently, benzyl bromoacetate (2.0 mL) was added at room temperature in portions, and the mixture was stirred for 4 hours. To the reaction mixture was added water, followed by extraction with ethyl acetate. This was washed with an aqueous saturated sodium chloride solution, dried with anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:3→0:1) to obtain the title compound (3.4 g) having the following physical property values.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09353113B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-2dc5b63d8e8140c19d7334c26d7ac4b1 |
| Source note | uspto-grants-2016_05 |