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Methyl iodide → (S)-2-Methoxy-3-phenylpropanoic acid

HRID 1482189
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HRID 1482189 반응식
[OH:1][C@@H:2]([CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[C:3]([OH:5])=[O:4].[H-].[Na+].[CH3:15]I>C1COCC1>[CH3:15][O:1][C@@H:2]([CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[C:3]([OH:5])=[O:4]
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 4447183-Phenyllactic acid, (S)-

생성물 1

HCID 11858535(S)-2-Methoxy-3-phenylpropanoic acid수율 65.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
65 °C

실험 절차

(S)-2-Hydroxy-3-phenylpropanoic acid (1.0 g, 6.02 mmol) was dissolved in THF (100 ml), sodium hydride (0.48 g, 12.00 mmol) and methyl iodide (1.71 g, 12.04 mmol) were added, and the mixture was stirred at 65° C. for one hour. After leaving to cool, the reaction solution was concentrated under reduced pressure and adjusted to pH 4 by adding a 6 M aqueous hydrochloric acid solution thereto. The aqueous layer was extracted with ethyl acetate, the organic layer was concentrated, and the resulting residue was purified by column chromatography (dichloromethane:methanol=10:1) to afford the title compound (0.71 g, 59%).

후처리

  1. customAfter leaving
  2. temperatureto cool
  3. concentrationthe reaction solution was concentrated under reduced pressure
  4. additionby adding a 6 M aqueous hydrochloric acid solution
  5. extractionThe aqueous layer was extracted with ethyl acetate
  6. concentrationthe organic layer was concentrated
  7. customthe resulting residue was purified by column chromatography (dichloromethane:methanol=10:1)

출처 및 근거

ORD 기록
ord-0b055f01eeec4ece90aa1dbb1d8ffac2
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409952B2

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