HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166617Generated: October 27, 2026
Cuminaldehyde → 1-Methoxy-2-[4-(1-methylethyl)phenyl]-ethene
https://huagongshe.com/reaction/1166617
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cuminaldehyde | HCID 326 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Methoxy-2-[4-(1-methylethyl)phenyl]-ethene | HCID 69421418 | 56.9% |
Reaction Steps
27.7 g of methoxymethyltriphenylphosphonium chloride is introduced into 350 ml of diethyl ether under nitrogen. At 0° C., 38.8 ml of n-butyllithium solution (1.6 M in hexane) is added in drops, and it is stirred for one hour at room temperature. 12 g of 4-isopropylbenzaldehyde in 50 ml of diethyl ether is now added, and it is stirred for one more hour. Sodium chloride solution is added to the reaction mixture, extracted with ethyl acetate, dried on sodium sulfate and concentrated by evaporation. After chromatography on silica gel with ethyl acetate/hexane, 8.1 g of 1-methoxy-2-[4-(1-methylethyl)phenyl]-ethene 42 (E,Z-mixture) is obtained as a colorless oil, which is dissolved in 200 ml of acetone and stirred under nitrogen with 10 ml of 2N hydrochloric acid overnight. Sodium chloride solution is added, extracted with ethyl acetate, dried on sodium sulfate and concentrated by evaporation. Chromatographic purification on silica gel with ethyl acetate/hexane yields 5.1 g of title compound 43 as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06613920B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-38776f80c3b04c1f9cbcece98ffdafb1 |
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| Source note | uspto-grants-2003_09 |
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