HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350864Generated: October 27, 2026
Potassium Hydroxide → [4-Tert-butyl-3-(2-methoxyethoxy)phenoxy]acetic acid
https://huagongshe.com/reaction/1350864
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl [4-tert-butyl-3-(2-methoxyethoxy)phenoxy]acetate | HCID 58640405 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [4-Tert-butyl-3-(2-methoxyethoxy)phenoxy]acetic acid | HCID 21097495 | 101.2% |
Reaction Steps
To a methanol (3 mL) solution of ethyl [4-tert-butyl-3-(2-methoxyethoxy)phenoxy]acetate (260 mg, 0.84 mmol) was added 2M potassium hydroxide solution (1 ml) at ambient temerature. The stirred mixture was refluxed at 90° C. for 30 minutes. The reaction mixture was then quenched with saturated aqueous solution of ammonium chloride and then crude products were extracted with ethyl acetate The organic layer was then washed with brine, dried over sodium sulfate. After filtration to separate solvent and sodium sulfate, the solvent was removed under reduced pressure to give a residue, which was applied to recrystallization from hexane to furnish 0.24 g (100% yield) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07214824B2 |
|---|
| Source dataset | uspto-grants-2007_05 |
|---|
| ORD ID | ord-f1ef786a100147e3a4436437773d405c |
|---|
| Source note | uspto-grants-2007_05 |
|---|