HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (6-((2,4-Dichlorobenzyl)oxy)-4,7-dimethyl-1-benzofuran-3-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl(6-((2,4-dichlorobenzyl)oxy)-4,7-dimethyl-1-benzofuran-3-yl)acetate | HCID 71721635 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-((2,4-Dichlorobenzyl)oxy)-4,7-dimethyl-1-benzofuran-3-yl)acetic acid | HCID 89768061 | 83.2% |
Reaction Steps
To a mixture of methyl(6-((2,4-dichlorobenzyl)oxy)-4,7-dimethyl-1-benzofuran-3-yl)acetate (147 mg), MeOH (2.0 mL) and THF (dry) (2.0 mL) was added 1N NaOH (1.12 mL) at room temperature. The mixture was stirred at room temperature for 2 h, and then concentrated in vacuo. The residue was neutralized with 1N HCl, and the mixture was extracted with EtOAc. The organic layer was washed with brine and, dried over MgSO4, and concentrated in vacuo. The precipitate was collected by filtration, and crystallized from EtOAc-hexane to give the title compound (118 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238639B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-7ca562ccaeaa456b87eb5a4a0031fedf |
| Source note | uspto-grants-2016_01 |