HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylpiperidine → 1-(2-Chloro-4-nitrobenzyl)-4-methylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylpiperidine | HCID 69381 | — |
| Reactant | alpha,2-Dichloro-4-nitrotoluene | HCID 3016511 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(2-Chloro-4-nitrobenzyl)-4-methylpiperidine | HCID 68816543 | — |
Reaction Steps
1 g (4.85 mmol) of 2-chloro-4-nitrobenzylchloride is slowly added dropwise to 2 mL (16.22 mmol) of 4-methylpiperidine at ambient temperature and the mixture is stirred for 15 minutes. The reaction mixture is diluted with ethyl acetate and extracted twice with water. The organic phase is dried over sodium sulfate and evaporated down. Yield: 1.3 g (99.7% of theory); C13H17ClN2O2 (M=268.74); calc.: molecular ion peak (M+H)+: 269/271; found: molecular ion peak (M+H)+: 269/271; Rf value: 0.4 (Alox, petroleum ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592373B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-68fe302d281a4c348e1ddba06fb81b3a |
| Source note | uspto-grants-2009_09 |