HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582756Generated: November 1, 2026
2-(2-Acetoxy-4-fluorophenoxy)ethanol → 2-(2-Hydroxy-4-fluorophenoxy)ethanol
https://huagongshe.com/reaction/1582756
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(2-Acetoxy-4-fluorophenoxy)ethanol | HCID 22718367 | — |
| Reactant | HCID 86597229 | HCID 86597229 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Hydroxy-4-fluorophenoxy)ethanol | HCID 22718235 | — |
Reaction Steps
2-(2-Acetoxy-4-fluorophenoxy)ethanol 1.53 g was dissolved in a mixed solvent of tetrahydrofuran 10 ml and water 5 ml, then lithium hydroxide monohydride 294 mg was added thereto, and the mixture was stirred at 90° C. After stirred for 10 hours, the reaction mixture was cooled and partitioned by adding water and ethyl acetate. The organic layer was washed with water and then with brine, dried over magnesium sulfate anhydride and evaporated. The residue was purified by silica gel column chromatography (hexane/ethyl acetate system), whereby the title compound (1.07 g, 80%) was obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06737425B1 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-12524f5734e5433b93ec789952030b17 |
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| Source note | uspto-grants-2004_05 |
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