HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (S)-1-(tert-butoxycarbonyl)-6-oxopiperidine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-(1,1-Dimethylethyl) (3R)-1,3-piperidinedicarboxylate | HCID 643516 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-1-(tert-butoxycarbonyl)-6-oxopiperidine-3-carboxylic acid | HCID 117690989 | 49% |
Reaction Steps
A solution of NaIO4 (5.6 g, 26 mmol) in water (30 mL) and RuCl3 (14 mg) were added to a solution of Boc-(R)-piperidine-3-carboxylic acid (1.5 g, 6.6 mmol) in EtOAc (30 mL). The reaction mixture was stirred overnight at ambient temperature. The two layers were separated and the aqueous phase was extracted with EtOAc (50 mL×3). The combined organic phases were washed with brine (50 mL×3), dried over anhydrous sodium sulfate, and concentrated. The residue was purified by flash column chromatography on silica gel (CH2Cl2/MeOH=20:1) to afford (S)-1-(tert-butoxycarbonyl)-6-oxopiperidine-3-carboxylic acid (790 mg, 49% yield) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434761B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-d9f44ceb39784ff4a5a8144d8d987207 |
| Source note | uspto-grants-2016_09 |