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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant3-(2-Ethoxyethoxy)-4-iodobenzaldehydeHCID 86626106—
ReactantMethyl (diethoxyphosphanyloxy)methoxyacetateHCID 86626110—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Productmethyl (Z)-3-[3-(2-ethoxyethoxy)-4-iodophenyl]-2-methoxyacrylateHCID 86626108—
Productmethyl (E)-3-[3-(2-ethoxyethoxy)-4-iodophenyl]-2-methoxyacrylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-60c1b6a724b645ca99a771d748a45c16
Source noteuspto-grants-2013_02