HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → 4-[2-(1-Ethoxycarbonyl-4-piperidyl)-ethyl]-2-phenyl quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Phenyl-4-(2-(4-piperidinyl)ethyl)quinoline | HCID 71219 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-[2-(1-Ethoxycarbonyl-4-piperidyl)-ethyl]-2-phenyl quinoline | HCID 12902716 | 104.4% |
Reaction Steps
A solution of 15.6 g of 2-phenyl-4-[2-(4-piperidyl)-ethyl]quinoline, prepared as indicated in Example 16, in 200 ml of chloroform is treated with stirring with 200 ml of a 1N aqueous solution of sodium hydroxide. Then 21.7 g of ethyl chloroformate are added, drop by drop, and the suspension obtained is stirred for 17 hours at the ambient temperature. After separation, the organic phase is washed with water, dried over magnesium sulphate, then evaporated under reduced pressure. 20 g of 4-[2-(1-ethoxycarbonyl-4-piperidyl)-ethyl]-2-phenyl-quinoline in the form of an oil are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04505916 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-ff04c08b5b7342ee88a1232240e7041a |
| Source note | uspto-grants-1985_03 |