HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458499Generated: October 26, 2026
4-(4'-Hydroxyphenyl)-2-butanone → HCID 23119605, compound
https://huagongshe.com/reaction/458499
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(4'-Hydroxyphenyl)-2-butanone | HCID 21648 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23119605 | HCID 23119605 | — |
Reaction Steps
The hapten [10-O-(carboxypropyl)]ractopamine ether(Hapten A—derivatised at position 10) was prepared in three steps according to FIG. 3 of the accompanying drawings, from 4-(4-hydroxyphenyl)-2-butanone, 2. The reaction of 4-(4-hydroxyphenyl)-2-butanone, 2 with ethyl 4-bromobutyrate in dimethylformamide (DMF) in the presence of sodium hydride (NaH), gives ethyl 4-[4-(3-oxobutyl)phenoxy]butanoate 3. The ketoester, 3, obtained was reacted with octopamine hydrochloride, 4, in methanol in the presence of triethylamine (TEA) and sodium cyanoborohydride (Na BH3CN) to give 10-O-[3-(ethoxycarbonyl)propyl]ractopamine ether 5, in moderate yields. The hapten A was obtained after saponification of the ester, 5, with sodium hydroxide (NaOH) (2N) in methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192722B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-aa8bb319c37c4ad38ea2d93a89e1cd4a |
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| Source note | uspto-grants-2007_03 |
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