HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 4-[Methyl-(3,3-dimethyl-7-isopropyl-2,3-dihydro-benzofuran-5-yl)-amino]-benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-[Methyl-(3,3-dimethyl-7-isopropyl-2,3-dihydro-benzofuran-5-yl)-amino]-benzoic acid ethyl ester | HCID 15454091 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[Methyl-(3,3-dimethyl-7-isopropyl-2,3-dihydro-benzofuran-5-yl)-amino]-benzoic acid | HCID 9862734 | 80% |
Reaction Steps
Following general procedure I and using 4-[methyl-(3,3-dimethyl-7-isopropyl-2,3-dihydro-benzofuran-5-yl)-amino]-benzoic acid ethyl ester (Compound 23, 0.03 g, 0.081 mmol) and 2 mL of 5M potassium hydroxide solution in 10 mL of ethanol, the title compound (0.022 g, 79%) was obtained as a white solid. 1H NMR (300 MHz, CDCl3): δ 7.90 (d, 2H, J=9.0 Hz), 6.85 (d, 1H, J=2.2 Hz), 6.78 (d, 1H, J=2.2 Hz), 6.63 (d, 2H, J=9.0 Hz), 4.27 (s, 2H), 3.33 (s, 3H), 3.09 (heptet, 1H, J=6.8 Hz), 1.33 (s, 6H), 1.23 (d, 6H, J=6.8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093838 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-c74778e13c5040f487d2d7eb1ba4c62b |
| Source note | uspto-grants-2000_07 |