HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247441Generated: October 29, 2026
Hydroxyamine hydrochloride → HCID 86594836, compound
https://huagongshe.com/reaction/2247441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 59218935 | HCID 59218935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86594836 | HCID 86594836 | — |
Reaction Steps
175 mg of Methyl (3′-acetyl-4′-methoxybiphenyl-3-yl)acetate was dissolved in 3 m of ethanol, then 55 mg of hydroxylamine hydrochloride and 65 mg of sodium acetate were added thereto, and the mixture was stirred at room temperature for 3 days. The reaction mixture was diluted with ethyl acetate and washed with 1N hydrochloric acid. The organic layer was dried over anhydrous magnesium sulfate and then filtered, and the filtrate was concentrated to give methyl [3′-(1-hydroxyiminoethyl)-4′-methoxybiphenyl-3-yl]acetate. This product was dissolved in 4 ml of ethanol, then 0.5 ml of 5N sodium hydroxide was added thereto, and the mixture was left at room temperature for 6 hours. The reaction mixture was neutralized with 1N hydrochloric acid and then extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and then filtered, and the filtrate was concentrated to give 166 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687664B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-6be92938496e4b64983ff5d5d9c6c76b |
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| Source note | uspto-grants-2010_03 |
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