HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295236Generated: October 30, 2026
Cyclopropyl methyl ketone → HCID 54225680, compound
https://huagongshe.com/reaction/2295236
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropyl methyl ketone | HCID 13004 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54225680 | HCID 54225680 | 89.7% |
Reaction Steps
A mixture of 4-fluorobenzaldehyde (9.30 g, 75.00 mmol, Aldrich) and cyclopropyl methyl ketone (6.30 g, 75.00 mmol) in absolute ethanol (100 ml) was treated with a solution of sodium ethoxide in ethanol (21% by weight solution; 2.79 ml, 7.50 mmol). After stirring for 2 hours at room temperature, additional 4-fluorobenzaldehyde was added (1.86 g, 15.00 mmol). The reaction mixture was stirred for 2 hours, concentrated to 1/3 volume and partitioned between 50% saturated NH4Ct/EtOAc (100 ml/250 ml). The layers were separated and the aqueous portion was extracted with EtOAc (twice) and the combined organics were washed with H2O (twice) and brine, dried (Na2SO4) and concentrated. The yellow oily residue was distilled (Vigroux column, bp 115°-120° C., 0.6 mm Hg) to afford the title compound as a colorless oil (12.8 g, 89.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05691322 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-46e54e2d35d645f790670a284044e54d |
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| Source note | uspto-grants-1997_11 |
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