HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731622Generated: October 31, 2026
Ethyl bromoacetate → HCID 13116829, compound
https://huagongshe.com/reaction/1731622
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13391436 | HCID 13391436 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13116829 | HCID 13116829 | — |
Reaction Steps
A mixture of 41.0 g (0.104 mol) of the R enantiomer of 2-[3-(2,6-dichloro-4-trifluoromethyl-phenoxy)phenoxy]-propionic acid, 15.8 g (0.114 mol) of potassium carbonate and 17.4 g (0.104 mol) of ethyl bromoacetate in 104 ml of acetonitrile was heated under reflux for 1 hour. Thereafter, working-up was carried out by filtering the reaction mixture under suction, evaporating down the filtrate, taking up the remaining residue in methylene chloride, and washing this solution once with water, drying it and then evaporating it down. The remaining residue was freed from residues of volatile constituents by gentle heating in a high vacuum. In this manner, 34.9 g (70% of theory) of the R enantiomer of (ethoxycarbonyl)-methyl 2-[3-(2,6-dichloro-4-trifluoromethylphenoxy)-phenoxy]-propionate were obtained in the form of a liquid having a refractive index nD20 =1.5190.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04622415 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-7904c68e05694a8687d3c30ba359e7ce |
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| Source note | uspto-grants-1986_11 |
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