HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen chloride-ethyl acetate → (3R)-3-(Methoxymethyl)-piperidine HCl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Reactant | tert-butyl (R)-3-methoxymethylpiperidine-1-carboxylate | HCID 58826553 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (3R)-3-(Methoxymethyl)-piperidine HCl | HCID 66795288 | — |
Reaction Steps
To a solution of tert-butyl (R)-3-methoxymethylpiperidine-1-carboxylate (13.00 g, 56.6 mmol) in ethyl acetate (26 ml) was added 4N HCl-ethyl acetate solution (26 ml), and the mixture was stirred at room temperature for 3 hr. The solvent was evaporated under reduced pressure to give (R)-3-methoxymethylpiperidine hydrochloride as a crude product. A mixed solvent (100 ml) of hexane:ethyl acetate=1:4 was added to the obtained solid, and the mixture was stirred. The solid was collected by filtration to give (R)-3-methoxymethylpiperidine hydrochloride (7.82 g, yield 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977331B1 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-b8ad4a45926745dd861b1e22cbff51dc |
| Source note | uspto-grants-2011_07 |