HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 1-[2-(4-Hydroxyphenylamino)benzoyl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 1-[2-(4-Methoxyphenylamino)benzoyl]piperidine | HCID 13505630 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[2-(4-Hydroxyphenylamino)benzoyl]piperidine | HCID 13505631 | 68.9% |
Reaction Steps
Boron tribromide (10 ml in 25 ml of methylene dichloride) was added dropwise over a 30 minute period to a solution of 15.5 g of 1-[2-(4-methoxyphenylamino)benzoyl]piperidine in 80 ml of dry methylene dichloride cooled in a bath of Dry Ice and isopropyl alcohol. The reaction mixture was allowed to warm to room temperature and to stand overnight. The solvent was then removed in vacuo, and the residue was treated with 100 ml of distilled water and made basic with about 250 ml of saturated sodium bicarbonate solution. The solid which formed was collected by filtration and recrystallized from ethanol to give 10.2 g of 1-[2-(4-hydroxyphenylamino)benzoyl]piperidine, colorless powder, m.p. 199°-201° C.(decompn.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04510139 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-e628529834754a4181ef70f7caa56e50 |
| Source note | uspto-grants-1985_04 |