HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → alpha-[[(2,4,6-Trimethoxyphenyl)amino]carbonyl]benzene acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | alpha-[[(2,4,6-Trimethoxyphenyl)amino]carbonyl] benzene acetic acid ethyl ester | HCID 10690735 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | alpha-[[(2,4,6-Trimethoxyphenyl)amino]carbonyl]benzene acetic acid | HCID 10665192 | — |
Reaction Steps
To a stirred solution of KOH (10.70 g, 0.191 mol) in absolute ethanol (1.1 L) was added α-[[(2,4,6-trimethoxyphenyl)amino]carbonyl] benzene acetic acid ethyl ester (55.28 g, 0.1480 mol), and the mixture was stirred for 41 hours. The resulting suspension was diluted with H2O (~900 mL) and rotoevaporated to remove ethanol. The solution was washed (ethyl acetate) and acidified with dropwise addition of 1M HCl (265 mL). The resulting precipitate was filtered off, washed (H2O), and dried in vacuo to give an off-white solid; yield 48.4 g (100%); 111°-113° C. (gas evolution).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05441975 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-4f82e0a201d247a48662a4833a625b1b |
| Source note | uspto-grants-1995_08 |