HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377307Generated: October 30, 2026
Ethyl Acetate → (E)-3-(4-Iodo-phenyl)-2-methyl-acrylic acid ethyl ester
https://huagongshe.com/reaction/2377307
Participants
| Role | Name | HCID | Charge |
|---|
| 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 | US07468391B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-3f3aa6f2138b4cada1eccc7635fd0632 |
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| Source note | uspto-grants-2008_12 |
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