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3-Fluorobenzaldehyde → 2-[(3-fluorophenyl)(hydroxy)methyl]-4-methoxy-N-methylbenzamide

HRID 2196385
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HRID 2196385 반응식
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:6]([C:7]([NH:9][CH3:10])=[O:8])=[CH:5][CH:4]=1.[Li]CCCC.[F:18][C:19]1[CH:20]=[C:21]([CH:24]=[CH:25][CH:26]=1)[CH:22]=[O:23]>C1COCC1>[F:18][C:19]1[CH:20]=[C:21]([CH:22]([OH:23])[C:11]2[CH:12]=[C:3]([O:2][CH3:1])[CH:4]=[CH:5][C:6]=2[C:7]([NH:9][CH3:10])=[O:8])[CH:24]=[CH:25][CH:26]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 680093-FluorobenzaldehydeHCID 3460314-methoxy-N-methylbenzamideHCID 178418339Butyllithium

생성물 1

HCID 685140052-[(3-fluorophenyl)(hydroxy)methyl]-4-methoxy-N-methylbenzamide

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a −78 C solution of 4-methoxy-N-methylbenzamide (2.0 g) in THF was added n-BuLi (10 mL, 2.5 M in hexanes). The reaction was stirred for 10 min at −78 C, warmed to 0 C, then cooled back to −78 C. 3-fluorobenzaldehyde (1.90 mL) was added as a solution in THF via cannula. The reaction was warmed to room temp, then quenched with saturated aqueous NH4Cl. The mixture was extracted with EtOAc, concentrated, and purified by flash chromatography (5% MeOH in CH2Cl2) to give 2-[(3-fluorophenyl) (hydroxy)methyl]-4-methoxy-N-methylbenzamide.

후처리

  1. temperaturewarmed to 0 C
  2. temperaturecooled back to −78 C
  3. customquenched with saturated aqueous NH4Cl
  4. extractionThe mixture was extracted with EtOAc
  5. concentrationconcentrated
  6. custompurified by flash chromatography (5% MeOH in CH2Cl2)

출처 및 근거

ORD 기록
ord-55dcba5398b54fcaafb57ab57cf1f501
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08338449B2

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