HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104489Generated: October 30, 2026
Ethylene Glycol → 3-Benzyl-4-phenyl-8-(trifluoromethyl)quinoline
https://huagongshe.com/reaction/2104489
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Phenyl[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]methanone | HCID 11360909 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Benzyl-4-phenyl-8-(trifluoromethyl)quinoline | HCID 11417167 | 54.2% |
Reaction Steps
Phenyl[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]methanone (Example 1, 0.244 g, 0.65 mmol) was taken into ethylene glycol (5 mL) along with hydrazine hydrate (0.3 mL) and heated at 120° C. for 2 hours. Next, a few pellets of KOH were added and reaction was heated at 180° C. for 4 hours. The reaction was allowed to cool to room temperature, where water was added and the mixture was extracted with ether and concentrated. The resulting material was purified via column chromatography using 5% ethyl acetate in hexane as the eluent to produce 0.128 g of desired product. MS (ESI) m/z 364 ([M+H]+); 1H NMR (CDCl3) δ 9.01 (s, 1H), 8.02 (d, J=7.2 Hz, 1H), 7.65 (d, J=7.6 Hz, 1H), 7.51 (m, 3H), 7.44 (m, 1H), 7.20 (m, 5H), 6.97 (m, 2H), 3.98 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07576215B2 |
|---|
| Source dataset | uspto-grants-2009_08 |
|---|
| ORD ID | ord-2f9bf6c7140f4b8695e533d5f20c5f82 |
|---|
| Source note | uspto-grants-2009_08 |
|---|