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Sodium Hydroxide → 5-Methoxy-6-(trifluoromethyl)indoline

HRID 840543
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반응식

HRID 840543 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[C:12]([F:15])([F:14])[F:13])[NH:8][CH:7]=[CH:6]2.C([BH3-])#N.[Na+].[OH-].[Na+]>C(O)(=O)C.O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[C:12]([F:15])([F:13])[F:14])[NH:8][CH2:7][CH2:6]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 14798Sodium HydroxideHCID 5003444Sodium cyanoborohydrideHCID 108225525-Methoxy-6-(trifluoromethyl)-1H-indole

생성물 1

HCID 112067135-Methoxy-6-(trifluoromethyl)indoline수율 99%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매

실험 절차

The indole (D2) (67.63 g, 0.315 mol) in glacial acetic acid (500 ml) was treated with sodium cyanoborohydride (40 g, 0.637 mol) portionwise at room temperature with stirring. After 3 h at room temperature the reaction mixture was diluted with water (500 ml) and basified with 40% aqueous NaOH with cooling. The mixture was then extracted with dichloromethane (3×500 ml) and the combined extracts were dried (Na2SO4) and evaporated to give the title compound (67.73 g, 99%) as an off-white solid.

후처리

  1. temperaturewith cooling
  2. extractionThe mixture was then extracted with dichloromethane (3×500 ml)
  3. dry with materialthe combined extracts were dried (Na2SO4)
  4. customevaporated

출처 및 근거

ORD 기록
ord-073aa94d19c44708b81e9e62e6c7d586
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06369060B1

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