HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919530Generated: November 3, 2026
Acetone → 5-(5'-Fluoro-2'-methoxyphenyl)pentanal
https://huagongshe.com/reaction/1919530
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-(5-Fluoro-2-methoxyphenyl)butanal | HCID 25258575 | — |
| Product | 5-(5'-Fluoro-2'-methoxyphenyl)pentanal | HCID 86623861 | 50% |
Reaction Steps
To a solution of 9 (0.46 g, 2.0 mmol) in acetone (20 mL) was added H2SO4 (5%, 2 mL) and the reaction was heated to reflux for 1.6 h. After the reaction was cooled to room temperature, most of the solvent was then removed in vacuo. A solution of NaHCO3 (sat. 40 mL) was added and the organics were extracted with EtOAc (3×40 mL) and the combined organic layers were washed with brine (30 mL) and dried over Na2SO4. The crude product obtained by removal of the solvent in vacuo was purified by flash column chromatography on silica (Rf=0.10, EtOAc/Hexane, 10:90, v:v) to give the product (0.20 g, 50%) as oil; 1H NMR (CDCl3, 500 MHz): δ 9.76 (s, 1 H), 6.88-6.82 (m, 2 H), 6.74 (dd, J=4.6, 8.6 Hz, 1 H), 3.79 (s, 3 H), 2.61 (t, J=7.3 Hz, 2 H), 2.45 (m, 2 H), 1.69-1.60 (m, 4 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08168635B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-7afb55c94d4248598f1d039f91af419a |
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| Source note | uspto-grants-2012_05 |
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