HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 69819234, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | methyl (2S)-piperidine-2-carboxylate hydrochloride | HCID 13246232 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69819234 | HCID 69819234 | — |
Reaction Steps
(2S)-Piperidine-2-carboxylic acid methyl ester hydrochloride (625 mg) was dissolved in dichloromethane. Then N,N-diisopropylethylamine (0.91 ml) and benzaldehyde (0.53 ml) were added to the solution at 0° C. After the whole was stirred for 30 minutes at the same temperature, sodium triacetoxyborohydride (1.48 g) was added. The reaction mixture was allowed to room temperature and stirred for 3 hours. The mixture was poured into aqueous saturated sodium hydrogen carbonate solution and extracted with ethyl acetate. The extract was dried over magnesium sulfate and evaporated under reduced pressure to give (2S)-1-benzylpiperidine-2-carboxylic acid methyl ester (795 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06787543B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-4ecc2fa5adaf41b2a186701f65308ae0 |
| Source note | uspto-grants-2004_09 |