HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985026Generated: November 2, 2026
Ethyl bromoacetate → HCID 68900879, compound
https://huagongshe.com/reaction/1985026
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | HCID 68901479 | HCID 68901479 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 68900879 | HCID 68900879 | — |
Reaction Steps
A methyl ethyl ketone mixture liquid of 1 equivalent of (1R)-1-(3-chlorophenyl)-2-[(1R,3R)-3-(3-hydroxyphenyl)cyclohexylamino]ethanol 1/3 toluene-solvate and from 2.0 to 3.0 equivalents of potassium carbonate was heated under reflux. With heating, a methyl ethyl ketone solution of from 1.0 to 1.2 equivalents of ethyl bromoacetate was dropwise added to the mixture liquid, and further heated under reflux for 3 to 4 hours. A part of the reaction liquid was sampled, and subjected to HPLC analysis. After cooled, this was filtered through Celite, and a methyl ethyl ketone solution of 1.0 equivalent of maleic acid was put into the obtained solution, and stirred. The precipitated crystal was taken out through filtration, and dried through aeration to obtain ethyl 3-[(1R,3R)-3-[(2R)-2-(3-chlorophenyl)-2-hydroxyethylamino]cyclohexyl]phenoxyacetate maleate. The obtained crystal was subjected to HPLC analysis, in which the content of (1R)-1-(3-chlorophenyl)-2-[(1R,3R)-3-(3-hydroxyphenyl)cyclohexylamino]ethanol (starting compound) and the content of ethyl 3-[(1R,3R)-3-[(2R)-2-(3-chlorophenyl)-2-hydroxyethylamino]cyclohexyl]phenoxyacetate (target product) in the crystal were determined according to the above-mentioned relative area percentage method.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07544841B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-52a996587da64933acda25c14659d239 |
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| Source note | uspto-grants-2009_06 |
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