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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCuminaldehydeHCID 326—
ReactantSodium ChlorideHCID 5234—
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product1-Methoxy-2-[4-(1-methylethyl)phenyl]-etheneHCID 6942141856.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613920B1
Source datasetuspto-grants-2003_09
ORD IDord-38776f80c3b04c1f9cbcece98ffdafb1
Source noteuspto-grants-2003_09