HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → cis-2-Methyl-4-phenylamino-3,4-dihydro-2h-quinoline-1-carboxylic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Methyl-4-phenylimino-3,4-dihydro-2H-quinoline-1-carboxylic Acid Benzyl Ester | HCID 12093187 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Solvent | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Product | cis-2-Methyl-4-phenylamino-3,4-dihydro-2h-quinoline-1-carboxylic acid benzyl ester | HCID 12093188 | 46.6% |
Reaction Steps
To a solution of 2-methyl-4-phenylimino-3,4-dihydro-2H-quinoline-1-carboxylic acid benzyl ester (16 g) in acetic acid (450 ml), sodium triacetoxyborohydride was added in small amounts (32.32 g), under stirring, at room temperature. The reaction mixture was then stirred at room temperature for one hour and poured on 1 liter of cold water under stirring. After precipitation, the mixture was filtered, dissolved in ethyl acetate and then, washed with water. The organic layer was separated and dried over sodium sulfate. The solvent was removed to give the crude compound (9g), recristallised in hot cyclohexane (40 ml), and then filtered at room temperature to give the desired compound (5.3 g, 46.6% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220760B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-1443954de1d64102a48a3d0065f448be |
| Source note | uspto-grants-2007_05 |