Benzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl ester → Ethyl 3-hydroxy-3-(4-methoxyphenyl)propanoate

HRID 133792

반응식

HRID 133792 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9](=[O:16])[CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:5][CH:4]=1.[BH4-].[Na+]>CO.S([O-])([O-])(=O)=O.[Na+].[Na+]>[OH:16][CH:9]([C:6]1[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:8][CH:7]=1)[CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12]

참가 물질

5

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온도
0 °C

실험 절차

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.

후처리

  1. additionAfter addition
  2. customto quench
  3. customthe reaction
  4. customMethanol was removed in vacuo, and water
  5. additionwas added to the residue
  6. dry with materialthe combined organic layers were dried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. customThe filtrate was evaporated in vacuo
  9. customThe crude mixture was purified by Flash Chromatography with eluent of 40% ethyl acetate/60% hexane

출처 및 근거

ORD 기록
ord-8116151a36d54ab390cb89a4201515d4
출처 데이터셋
uspto-grants-2008_06
특허 번호
US07390925B2

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