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HRID 133792作成日:2026年10月27日
Benzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl ester → Ethyl 3-hydroxy-3-(4-methoxyphenyl)propanoate
https://huagongshe.com/reaction/133792
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 | Sodium borohydride | HCID 4311764 | — |
| 触媒 | Sodium Sulfate | HCID 24436 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Ethyl 3-hydroxy-3-(4-methoxyphenyl)propanoate | HCID 11096232 | 56.2% |
反応手順
A solution of ethyl 3-(4-methoxyphenyl)-3-oxopropanoate (444 mg, 2 mmol) in methanol (4 mL) was added sodium borohydride (76 mg, 2.0 mmol) at 0° C. slowly. After addition, the reaction mixture was stirred at 0° C. for 30 min. Two drops of saturated sodium sulfate solution were added to the reaction mixture to quench the reaction. Methanol was removed in vacuo, and water was added to the residue. The aqueous solution was extrated with ethyl acetate (x3), and the combined organic layers were dried over anhydrous sodium sulfate, and filtered. The filtrate was evaporated in vacuo. The crude mixture was purified by Flash Chromatography with eluent of 40% ethyl acetate/60% hexane to give the title compound as a clear oil (252 mg, 56% yield). 1H NMR (400 MHz, CDCl3) δ 1.22-1.28 (m, 3 H) 2.63-2.75 (m, 2 H) 3.79 (s, 3 H) 4.16 (q, J=7.13 Hz, 2 H) 5.07 (dd, J=9.06, 3.78 Hz, 1 H) 6.85-6.89 (m, 2 H) 7.24-7.31 (m, 2 H). HPLC retention time: 1.973 min (method A). MS (ESI) (M+Na)+ 246.96.
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-8116151a36d54ab390cb89a4201515d4 |
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| 出典メモ | uspto-grants-2008_06 |
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