HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Catalyst | Palladium barium sulphate | HCID 17887766 | — |
| Catalyst | Lindlars catalyst | HCID 131709914 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Quinoline | HCID 7047 | — |
Reaction Steps
This step is a step for obtaining compound (2-5) by reducing the triple bond of compound (2-4) to a double bond. Compound (2-5) can be obtained by using a catalyst such as Lindlar's catalyst, palladium-barium sulfate or the like in a solvent such as tetrahydrofuran, ethyl acetate, acetonitrile, methanol, ethanol or the like and under a hydrogen atmosphere. A preferable solvent is ethyl acetate. In order to obtain a favorable result, 0.1 to 1 equivalent of quinoline may be added with respect to compound (2-4). A catalytic amount to an excess of catalyst is used with respect to compound (2-4). The reaction temperature is room temperature, the reaction time is from 15 minutes to 24 hours, and the reaction pressure is from 1 to 4 atmospheres.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829585B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-a33aed9739c049d1930d1a873d5f0bea |
| Source note | uspto-grants-2010_11 |