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HRID 1869448作成日:2026年10月25日

Triethyl phosphonoacetate → ethyl-E-4-(3-methoxyphenyl)-4-methylpent-2-enoate

https://huagongshe.com/reaction/1869448

反応式

関与物質

役割名称HCID仕込み量
反応物Triethyl phosphonoacetateHCID 13345—
反応物Ammonium ChlorideHCID 25517—
反応物Lithium diisopropylamideHCID 2724682—
反応物2-(3-Methoxyphenyl)-2-methylpropanalHCID 13296993—
溶媒TetrahydrofuranHCID 8028—
溶媒Tetrahydrofuran heptane ethylbenzolHCID 22742125—
生成物ethyl-E-4-(3-methoxyphenyl)-4-methylpent-2-enoateHCID 8659993195.8%

反応手順

33.6 g (114.3 mmol) of phosphonoacetic acid triethyl ester is introduced into 148 ml of tetrahydrofuran. At 0° C., 79.7 ml of a 2 M solution of LDA in THF/heptane/ethylbenzene is added in drops (1½ hours). After one hour of stirring, 24.3 g (136.34 mmol) of 2-(3-methoxyphenyl)-2-methylpropanal, dissolved in 130 ml of tetrahydrofuran, is added in drops at 0° C. After five days of stirring at room temperature, the reaction mixture is poured into 250 ml of dilute ammonium chloride solution and extracted twice with 400 ml each of diethyl ether. The combined organic extracts are treated as usual, and the residue that is obtained is chromatographed on silica gel (mobile solvent ethyl acetate/hexane). 27.2 g (80.4%) of the desired compound is isolated.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07638515B2
出典データセットuspto-grants-2009_12
ORD IDord-a6c56cfdff1a452ab8f8c13c4eed5ba2
出典メモuspto-grants-2009_12