HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 3-(N-Propyl)amino-1,2,3,4-tetrahydroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-(N-Propionyl)amino-1,2,3,4-tetrahydroquinoline | HCID 19697664 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(N-Propyl)amino-1,2,3,4-tetrahydroquinoline | HCID 22034088 | 89.6% |
Reaction Steps
To a ice-cooled solution of 3.2 g (15.6 mmol) 3-(N-propionyl)amino-l,2,3,4-tetrahydroquinoline in 50 ml dry diethyl ether and 80 ml dry tetrahydrofurane was 3.0 g (79 mmol) lithium aluminum hydride added. The mixture was gently heated to reflux and kept that way for 5 days. Ethyl acetate (4.5 ml), 3.0 ml water,3.0 ml 15% sodium hydroxide and 9 ml water was added consecutively. The precipitate appearing after 5 minutes was filtered off and washed with diethyl ether. Evaporation of the etheric solution yielded 2.66 g (89%) of the desired product.: 13C NMR () d 11 (76), 23.46, 33.71, 46.41, 48.98, 50.43, 113.79, 117.29, 119.37, 126.87, 130.06, 144.09; MS m/e 190 (M+, 17), 132 (100), 130 (32), 72 (22), 118 (17), 131 (17).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05461061 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-80b333584b104ce99ff56cdf9a33ce9e |
| Source note | uspto-grants-1995_10 |