HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinaldic Acid → 1-(Quinolin-2-yl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinaldic Acid | HCID 7124 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Quinolin-2-yl)ethan-1-one | HCID 318703 | 40% |
Reaction Steps
Quinaldic acid (2.76 grams, 0.017 mole) was dissolved in 100 ml of dried tetrahydrofuran. Then 25 ml of 1.6 M (0.04 mole) of methyl lithium was added using a syringe. Reaction appeared immediate. The solution was stirred and heated under reflux for two hours and then poured into 600 ml of ice water. The ketone (2-acetylquinoline) was extracted with four 25 ml portions of ethyl ether which, after drying, was removed by rotary evaporation to yield ca. 1.0 g (ca. 40%) of 2-acetylquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04440771 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-8e603d5c5f644adf84f0b4b685ac973e |
| Source note | uspto-grants-1984_04 |