HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 4-(2-fluorophenyl)piperidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 20511804 | HCID 20511804 | — |
| Product | Ethyl 4-(2-fluorophenyl)piperidine-4-carboxylate | HCID 20511806 | 68.4% |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
A mixture of 35.8 parts of 4-(2-fluorophenyl)-1-(4-methylphenylsulfonyl)-4-piperidinecarbonitrile and 50 parts of a sulfuric acid solution 75% is stirred for 4 hours at about 150° C. 192 Parts of ethanol are added dropwise. Upon completion, stirring is continued for 5 hours at reflux temperature. The reaction mixture is cooled and poured onto crushed ice. The whole is alkalized with ammonium hydroxide and the product is extracted with dichloromethane. The extract is dried, filtered and evaporated, yielding 17.2 parts (68.4%) of ethyl 4-(2-fluorophenyl)-4-piperidinecarboxylate as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04369184 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-31ab281da44e465ab89ea166468b19f4 |
| Source note | uspto-grants-1983_01 |