HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloroethyl chloroformate → 4-(2-Chlorophenyl)-4-methylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | HCID 15469930 | HCID 15469930 | — |
| Reactant | HCID 18675725 | HCID 18675725 | — |
| Reactant | HCID 23136891 | HCID 23136891 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(2-Chlorophenyl)-4-methylpiperidine | HCID 23136982 | — |
Reaction Steps
The mixture of 1-benzyl-4-(2-chloro-phenyl)-4-methylpiperidine and 1-benzyl-4-(4-chloro-phenyl)-4-methyl-piperidine (1.6 g) was dissolved in methanol (30 mL) and 1-chloroethylchloroformate (0.9 mL) was added. The mixture was heated at reflux for 10 minutes and allowed to cool. The solvent was removed by evaporation under vacuum and the residue precipitated from ethyl acetate with ether to give a 4:1 mixture of the title compound and 4-(4-chloro-phenyl)-4-methyl-piperidine which was used directly without further purification. LCMS m/z 210.2 [M+H]+. R.T.=2.64 min (Analytical Method 4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642621B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-4efed432bd794affafebc2c42892db68 |
| Source note | uspto-grants-2014_02 |