HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460839Generated: October 29, 2026
Acetone → 2-(4-Fluorophenoxy)acetaldehyde
https://huagongshe.com/reaction/460839
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1-(2,2-Diethoxyethoxy)-4-fluorobenzene | HCID 11447518 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Fluorophenoxy)acetaldehyde | HCID 11051869 | 94% |
Reaction Steps
A mixture of 4-fluorophenoxyacetaldehyde diethyl acetal (30.0 g., 0.131 mole) acetone (150 ml.), water (150 ml.), and concentrated sulfuric acid (0.8 ml.) is refluxed overnight (ca. 16 hours). The mixture is allowed to cool to room temperature, and is then extracted with methylenechloride four times. The combined extracts are washed with aqueous sodium bicarbonate and dried over anhydrous magnesium sulfate. The solvent is stripped off on a rotary evaporator and the oil residue is subsequently distilled in vacuo at 70°/0.05 mm to give the title compound (19.0 g., 0.123 mole, 94%). ir (neat) 3.23, 3.50, 3.63, 5.71, 6.62, 7.00, 8.00, 8.24, 9.07, 9.38, 12.03, 12.51, 13.12μ; pmr (CCl4) δ 4.37 (2H, d, J=1Hz), 6.6-7.1 (4H, m), 9.68 (1H, t, J=1Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04061643 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-50641f48493e4ba9a5b568f60b1c952e |
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| Source note | uspto-grants-1977_12 |
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