HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (S)-Methyl piperidine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Pipecolic acid, (-)- | HCID 439227 | — |
| Product | (S)-Methyl piperidine-2-carboxylate | HCID 853680 | 56% |
Reaction Steps
To a mixture of (S)-piperidine-2-carboxylic acid (10 mmol, 1.29 g) in MeOH (20 mL) is dropwise added thionyl chloride (30 mmol, 2.17 mL) at room temperature. The mixture is stirred at 2 hours, and then concentrated under reduced pressure. To the residue is added water (5 mL) and basified with potassium carbonate. The mixture is extracted with CH2Cl2. The combined organic layer is dried over Na2SO4, filtrated, and concentrated under reduced pressure to give (S)-piperidine-2-carboxylic acid methyl ester as a pale brown oil (800 mg, 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759365B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-0cdca4ad2b6240f19189e7439f27417c |
| Source note | uspto-grants-2014_06 |