HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390673Generated: October 30, 2026
Water → methyl (Z)-3-[3-(2-ethoxyethoxy)-4-iodophenyl]-2-methoxyacrylate
https://huagongshe.com/reaction/390673
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(2-Ethoxyethoxy)-4-iodobenzaldehyde | HCID 86626106 | — |
| Reactant | Methyl (diethoxyphosphanyloxy)methoxyacetate | HCID 86626110 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | methyl (Z)-3-[3-(2-ethoxyethoxy)-4-iodophenyl]-2-methoxyacrylate | HCID 86626108 | — |
| Product | methyl (E)-3-[3-(2-ethoxyethoxy)-4-iodophenyl]-2-methoxyacrylate | HCID 86626109 | — |
Reaction Steps
0.30 g (7.5 mmol) of sodium hydride is added portionwise to a solution at 0° C. of 1.80 g (7.5 mmol) of methyl (diethoxyphosphanyloxy)methoxyacetate (prepared according to Example 24b) in 20 mL of tetrahydrofuran. The reaction mixture is stirred for 45 minutes at room temperature and then 2 g (6.25 mmol) of 3-(2-ethoxyethoxy)-4-iodobenzaldehyde (prepared according to Example 38c) in 10 mL of tetrahydrofuran. The reaction is slightly exothermic, and the reaction mixture is maintained at a temperature of 25-30° C. with an ice-water bath. When the temperature has stabilized, the reaction mixture is stirred for 24 hours at room temperature. After addition of 50 mL of water and extraction with ethyl acetate, the organic phases are combined, washed with saturated sodium chloride solution, dried over sodium sulfate and evaporated. The crude product obtained is purified by chromatography on a column of silica eluted with a 95/5 heptane/ethyl acetate mixture to give 411 mg of methyl (Z)-3-[3-(2-ethoxyethoxy)-4-iodophenyl]-2-methoxyacrylate and 526 mg of methyl (E)-3-[3-(2-ethoxyethoxy)-4-iodophenyl]-2-methoxyacrylate in the form of colorless oils.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383652B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-60c1b6a724b645ca99a771d748a45c16 |
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| Source note | uspto-grants-2013_02 |
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