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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methyl hept-6-en-2-ynoate | HCID 59644062 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (Z)-Methyl 3-Methylhepta-2,6-dienoate | HCID 59644092 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039465B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-eb59f0ed371d4fb4b3b0354ea76a7b3d |
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| Source note | uspto-grants-2011_10 |
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