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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664253Generated: October 30, 2026

Ethanol → (Z)-Methyl 3-Methylhepta-2,6-dienoate

https://huagongshe.com/reaction/1664253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethyl hept-6-en-2-ynoateHCID 59644062—
ReactantHCID 178418348HCID 178418348—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(Z)-Methyl 3-Methylhepta-2,6-dienoateHCID 59644092100%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A suspension of copper(I) iodide (12.38 g, 65 mmol) in 150 mL of dry THF under a nitrogen atmosphere was cooled to −20° C., and methyllithium (1.6 M in ether, 81.5 mL, 130 mmol) was added dropwise over 15 min. The solution was cooled to −78° C., and 4.49 g (32.5 mmol) of the compound from Example 19 in 15 mL of dry THF was added gradually, keeping the temperature below −70° C. After 1 h, 40 mL of ethanol was added cautiously, and the mixture was allowed to warm to room temperature. The mixture was diluted with ether, and washed with satd aq NH4Cl (200 mL), 5N NH3 (4×250 mL), water (200 mL), and brine (200 mL), dried, and the bulk of the solvent was evaporated to give the title compound (6.8 g, 100%) as an oil. The material had only minor solvent contamination and was adequate for use in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039465B2
Source datasetuspto-grants-2011_10
ORD IDord-eb59f0ed371d4fb4b3b0354ea76a7b3d
Source noteuspto-grants-2011_10