HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 6-Amino-4,5,8-trimethylquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 4,5,8-Trimethyl-6-nitroquinoline | HCID 10560662 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Amino-4,5,8-trimethylquinoline | HCID 15380018 | — |
Reaction Steps
A mixture of 6-nitro-4,5,8-trimethylquinoline (0.60 g), tin(II)chloride dihydrate (3.13 g), and ethanol (40 mL) is heated for 3 hours at 60°-65° C. and then cooled to room temperature. 10% Aqueous sodium hydroxide (24 mL) and water (48 mL) are added, and the mixture is extracted three times with chloroform. The combined organic layers are washed with saturated sodium bicarbonate solution, dried over sodium sulfate, filtered and evaporated to afford a crude product. The crude product is purified by flash chromatography using 25% ethyl acetate in hexane as eluent, providing 6-amino-4,5,8-trimethylquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05578607 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-b7cb0d2c55c1455391da6faebe32e7c7 |
| Source note | uspto-grants-1996_11 |