HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384124Generated: October 29, 2026
Hydrochloric Acid → HCID 86641944, compound
https://huagongshe.com/reaction/384124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydroxylamine HCl | HCID 21645 | — |
| Reactant | HCID 68430400 | HCID 68430400 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86641944 | HCID 86641944 | — |
Reaction Steps
To a solution of ethyl 3-oxo-4-(4-((2-phenoxybenzyl)oxy)phenyl)butanoate (40 mg) in 1,4-dioxan (0.12 ml), 9 mg of hydroxylammonium chloride and 0.1 ml of 2.5N sodium hydroxide were added under ice-cooling, and the reaction solution was stirred at 0° C. for 1.5 hours. Concentrated hydrochloric acid (0.07 ml) was further added, and the reaction solution was stirred at room temperature for 20 minutes. The reaction solution was extracted with chloroform, the combined organic layers were washed with a saturated saline solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue obtained was purified by preparative thin layer chromatography (Kieselgel™ 60 F254, Art5744, made by Merck & Co., hexane/ethyl acetate (1:1) to afford the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367708B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-7919e7a9044349a1b93bd5e75c6d3379 |
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| Source note | uspto-grants-2013_02 |
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