HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → HCID 9957700, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21867230 | HCID 21867230 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 9957700 | HCID 9957700 | — |
Reaction Steps
Methyl[3,5-dibromo-4-(2-phenyl-5-benzofuranyloxy)phenyl]acetate (200 mg) was diluted in ethanol (2 mL) and treated with an aqueous saturated solution of potassium hydroxide (0.5 mL). The reaction mixture was refluxed for 1.5 hours. The reaction mixture was concentrated, diluted with chloroform and washed with an aqueous solution of hydrochloric acid (1 N). The organic phase was dried over magnesium sulphate, filtered and concentrated. This gave 0.13 g (70%) of 3,5-dibromo-4-(2-phenyl-5-benzofuranyloxy)-phenylacetic acid as a beige solid mass. 1H-NMR (300 MHz, DMSO-d6): δ 12.5 (br s, 1H), 7.86 (d, J=7.2 Hz, 2H), 7.34 (s, 2H), 7.61 (d, J=8.4 Hz, 1H), 7.50 (t, J=5.1 Hz, 3H), 7.42 (d, J=7.1, 1H), 7.35 (s, 1H), 6.87 (s, 1H), 3.70 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07144909B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-3c52d5f650e2430098e23586acc92ea6 |
| Source note | uspto-grants-2006_12 |