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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444534Generated: October 25, 2026

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

https://huagongshe.com/reaction/1444534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-(3-Methoxyphenyl)-2-methylpropanalHCID 13296993—
SolventTetrahydrofuranHCID 8028—
SolventTetrahydrofuran heptane ethylbenzolHCID 22742125—
Productethyl-E-4-(3-methoxyphenyl)-4-methylpent-2-enoateHCID 8659993195.8%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662821B2
Source datasetuspto-grants-2010_02
ORD IDord-df5b3e0ccc6e4faa86fa856cacba9f74
Source noteuspto-grants-2010_02