HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765700Generated: October 30, 2026
Ethyl Acetate → (E)-3-(4-Iodo-phenyl)-2-methyl-acrylic acid ethyl ester
https://huagongshe.com/reaction/1765700
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Iodobenzaldehyde | HCID 96657 | — |
| Reactant | Triethyl-2-phosphonopropionate | HCID 92003523 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (E)-3-(4-Iodo-phenyl)-2-methyl-acrylic acid ethyl ester | HCID 57424206 | 99% |
Reaction Steps
A stirred, cooled (−78° C.) solution of triethyl-2-phosphonopropionate (10 g, 41.9 mmol) in anhydrous tetrahydrofuran (100 mL) was treated with a 1.6M solution of n-butyl lithium in hexanes (25 mL, 40 mmol). After 10 min, the reaction mixture was cannulated into a cooled (−78° C.) solution of 4-iodo-benzaldehyde (4.66 g, 20 mmol) in tetrahydrofuran (25 mL). After 30 minutes, it was quenched with saturated aqueous ammonium chloride solution and extracted with diethyl ether (×2). The combined organic phase was dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford an oil that was subjected to flash column chromatography over silica gel (230–400 mesh) using 9–10% ethyl acetate in hexane as the eluent to afford the title compound (6.3 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07226951B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-593d708ceb45495cbc3fefd14ff79672 |
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| Source note | uspto-grants-2007_06 |
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