HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2-(4-(Quinolin-2-ylmethoxy)phenyl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 2-(4-(quinolin-2-ylmethoxy)phenyl)acetate | HCID 58368005 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-(Quinolin-2-ylmethoxy)phenyl)acetic acid | HCID 14500235 | 95.8% |
Reaction Steps
To a stirred solution of ethyl 2-(4-(quinolin-2-ylmethoxy)phenyl)acetate (38.0 g, 106.741 mmol) in ethanol (200 mL) and water (100 mL) was added KOH (23.9 g, 426.964 mmol) at room temperature. The mixture was stirred at RT for 4 h and after complete consumption of starting material as monitored by TLC, the reaction mixture was diluted with water (50 mL) and acidified using 1 N HCl at 0° C., The aqueous layer was extracted with EtOAc (2×150 mL) and the combined organic extracts were washed with water (50 mL) and brine (50 mL), dried over anhydrous Na2SO4, and evaporated in vacuo to afford 2-(4-(quinolin-2-ylmethoxy)phenyl)acetic acid (30.0 g, 95%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09265767B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-676472f2cc394744b6d426de41df83fa |
| Source note | uspto-grants-2016_02 |