HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397184Generated: October 27, 2026
Potassium Hydroxide → Rac-cyclohexyloxy-(3,4-dichloro-phenyl)-acetic acid
https://huagongshe.com/reaction/397184
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Rac-cyclohexyloxy-(3,4-dichloro-phenyl)-acetic acid methyl ester | HCID 67484331 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Rac-cyclohexyloxy-(3,4-dichloro-phenyl)-acetic acid | HCID 12044175 | 97% |
Reaction Steps
A solution of rac-cyclohexyloxy-(3,4-dichloro-phenyl)-acetic acid methyl ester (527 mg, 1.66 mmol) in ethanol (15 mL) was treated with a solution of potassium hydroxide (233 mg, 4.15 mmol) in water (2 mL) and the mixture was stirred at 25° C. After 3 h, the reaction was diluted with water (5 mL), and the ethanol was removed in vacuo. The aqueous layer was then acidified to pH 2 with 1N hydrochloric acid and extracted with dichloromethane (3×15 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residual oil was purified by flash chromatography (Merck Silica gel 60, 230-400 mesh, 95/5 chloroform/methanol plus 1% acetic acid) to give rac-cyclohexyloxy-(3,4-dichloro-phenyl)-acetic acid (487 mg, 97% yield) as a colorless oil: EI-HRMS m/e calcd for C14H16Cl2O3 (M+) 302.0477, found 302.0486.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06608218B2 |
|---|
| Source dataset | uspto-grants-2003_08 |
|---|
| ORD ID | ord-c4f53e1828c54b8f8052a1bf4a1a5ab2 |
|---|
| Source note | uspto-grants-2003_08 |
|---|