HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717761Generated: October 31, 2026
Acetone → 3-(4-fluorophenyl)-6-methyl-N-(propan-2-ylidene)-3,4-dihydroquinolin-1(2H)-amine
https://huagongshe.com/reaction/717761
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-(4-Fluorophenyl)-6-methyl-1-nitroso-1,2,3,4-tetrahydroquinoline | HCID 86691922 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Product | 3-(4-fluorophenyl)-6-methyl-N-(propan-2-ylidene)-3,4-dihydroquinolin-1(2H)-amine | HCID 86691923 | 92.7% |
Reaction Steps
To a stirred solution of 3-(4-fluorophenyl)-6-methyl-1-nitroso-1,2,3,4-tetrahydroquinoline (0.28 g, 0.00103 mol) in acetone (15 mL) was added saturated ammonium chloride solution (0.6 mL), and water (0.6 mL) at RT. The resulting brown colored reaction mixture was cooled to 15° C. Zinc dust (0.269 g, 0.00414 mol) was added portionwise at the same temperature, and after the addition, the reaction mixture was stirred for 1 h at RT. The reaction was monitored by TLC. After completion, solvent was removed under reduced pressure and the residue extracted with EtOAc (3×100 mL). The organic layer was dried over anhydrous sodium sulfate, solvent was removed under reduced pressure to obtain product as a brown colored oil (0.27 g, 92.7% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193728B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-3fb64ff3af674e98a78a6fe3dea274cf |
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| Source note | uspto-grants-2015_11 |
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