HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081310Generated: November 2, 2026
Ethyl Acetate → 2-[4-(2-butyl-1-benzofuran-3-carbonyl)-2,6-diiodophenoxy]acetic acid
https://huagongshe.com/reaction/1081310
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2-Butylbenzofuran-3-yl) (4-hydroxy-3,5-diiodophenyl) ketone | HCID 74769 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-[4-(2-butyl-1-benzofuran-3-carbonyl)-2,6-diiodophenoxy]acetic acid | HCID 10897325 | 49.7% |
Reaction Steps
A mixture of 2-n-butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran 1.0 g (1.83 mmol) and potassiumcarbonate 0.56 g (4 mmol) in aceton (dry) 100 ml, α-brom ethylacetate 1.0 g (12 mmol was added, and the solution was extracted with 100 ml water. The organic layer was evaporated to dryness and the yellow rest was dissolved in methanol 50 ml+1M NaOH 50 ml. The solution was heated to 50° C. for 15 h, extracted with 3×75 ml dichloromethane, and dried (MgSO4). Evaporating the solution and purification on silica gave 0.55 g (005).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05585404 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-36b37858151a42fd8facdaf2a2abe40d |
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| Source note | uspto-grants-1996_12 |
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