HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylpiperidine → HCID 14208556, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylpiperidine | HCID 12291 | — |
| Reactant | 3-Phenylpropylamine | HCID 16259 | — |
| Reactant | HCID 14208554 | HCID 14208554 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14208556 | HCID 14208556 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
The title product of Example 2 (7.4 g, 17.9 mmol) dissolved in 75 ml of CH2Cl2 was flushed with Ar and cooled to 0° C. N-methylpiperidine (NMP, 2.2 ml, 17.9 mmol) was added to the reaction before it was cooled to -78° C. and charged with 2.5 ml (17.9 mmol) of IBCF. The reaction was allowed to warm to -15°, maintained at this temperature for 15 min., cooled to -78°, and charged with 2.4 g (17.9 mmol) of 3 phenylpropyl amine (PPA). The crude product, obtained after a reaction work up by the method of Example 1, was chromatographed on a Waters prep 500 using a Porasil cartridge eluting with 2% to 3% ethanol (EtOH)/CH2Cl2. The title product was obtained as a white solid (4.54 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04757153 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-f5e799514a6844a4826c7a334d3bbbe5 |
| Source note | uspto-grants-1988_07 |