HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 3-(2-Quinolinylmethoxy)benzeneacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Acetylresorcinol | HCID 5055 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Chloromethyl)quinoline | HCID 20394 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Product | 3-(2-Quinolinylmethoxy)benzeneacetic acid | HCID 128543 | — |
Reaction Steps
A mixture of 2-chloromethyl quinolin (2.3 g, 13.3 mmol), 3-hydroxyphenyl acetate (2.2 g, 13.3 mmol), excess powdered potassium carbonate (10 g) and a catalytic amount of potassium iodide (0.1 g) in dry acetone (150 ml) was refluxed overnight (18 hr.). The reaction mixture was filtered, and the filtrate was concentrated, taken up in ethyl acetate, and the organic extract was washed with a 5% NaOH solution and brine. After drying over MgSO4, all volatiles were removed from the organic extract, and the crude oil was chromatographed on silica gel (20% ethylacetate in hexanes) to obtain the methyl ester of the desired product (3.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04794188 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-19d90a457c5d4b94bcb767515013d16d |
| Source note | uspto-grants-1988_12 |