HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (7-Chloro-6-((2,4-dichlorobenzyl)oxy)-1-benzofuran-3-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl(7-chloro-6-((2,4-dichlorobenzyl)oxy)-1-benzofuran-3-yl)acetate | HCID 118667011 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (7-Chloro-6-((2,4-dichlorobenzyl)oxy)-1-benzofuran-3-yl)acetic acid | HCID 89768195 | 87.1% |
Reaction Steps
To a mixture of methyl(7-chloro-6-((2,4-dichlorobenzyl)oxy)-1-benzofuran-3-yl)acetate (218.9 mg), MeOH (2.0 mL) and THF (dry) (2.0 mL) was added 1N NaOH (1.643 mL) at room temperature. The mixture was stirred at room temperature for 2 h. The residue was concentrated. The residue was neutralized with 1N HCl, and the mixture was extracted with EtOAc. The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The precipitate was collected by filtration, and crystallized from EtOH-hexane to give the title compound (184 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238639B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-84c93ce63f6846dcb6dc17b4e70d92c5 |
| Source note | uspto-grants-2016_01 |