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HRID 133788作成日:2026年10月27日
Benzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl ester → Ethyl 3-(methoxyimino)-3-(4-methoxyphenyl)propanoate
https://huagongshe.com/reaction/133788
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl ester | HCID 76150 | — |
| 反応物 | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Ethyl 3-(methoxyimino)-3-(4-methoxyphenyl)propanoate | HCID 58984518 | — |
反応手順
A mixture of ethyl 3-(4-methoxyphenyl)-3-oxopropanoate (500 mg) and MeONH2.HCl (207 mg) in ethanol (4 mL) was heated at 80° C. for 2 h. Ethanol was removed in vacuo, and saturated sodium bicarbonate was added to the residue. The aqueous solution was extrated with ethyl acetate (x4), and the combined organic layers were washed with brine, dried over anhydrous sodium sulfate, and filtered. The filtrate was evaporated in vacuo to give the title compound as a colorless oil, which was used directly in the Step B. HPLC retention time: 2.02 min (method A). MS (ESI) (M+H)+ 252.14.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07390925B2 |
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| 出典データセット | uspto-grants-2008_06 |
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| ORD ID | ord-5d0270f549334feb8b9e66f55faeee5c |
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| 出典メモ | uspto-grants-2008_06 |
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