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Sodium → 4-methoxy-5-methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole

HRID 623689
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HRID 623689 반응식
[Na].[CH3:2][O-:3].[Na+].F[B-](F)(F)F.CO[N+:12]1[N:13]([C:18]2[CH:23]=[CH:22][C:21]([C:24]([F:27])([F:26])[F:25])=[CH:20][CH:19]=2)[N:14]=[C:15]([CH3:17])[CH:16]=1>CO.O>[CH3:2][O:3][C:16]1[C:15]([CH3:17])=[N:14][N:13]([C:18]2[CH:19]=[CH:20][C:21]([C:24]([F:25])([F:26])[F:27])=[CH:22][CH:23]=2)[N:12]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 5360545SodiumHCID 10942334Sodium MethoxideHCID 901113321-Methoxy-4-methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazolium tetrafluoroborate2회

생성물 1

HCID 901117224-methoxy-5-methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole

시약·촉매·용매 2

HCID 887Methanol용매
HCID 962
Water
용매

반응 조건

온도
23 °C

실험 절차

Sodium metal (0.25 g, 11.0 mmol) was stirred at 23° C. in methanol (10 mL) until a clear solution was obtained. This sodium methoxide solution was added to crude 1-methoxy-4-methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazolium tetrafluoroborate (1:1) (i.e. the product of Step B, 1.1 g, 3.2 mmol). The reaction mixture was stirred at 23° C. for 6 h, during which time a white precipitate formed. The reaction mixture was diluted with water (20 mL) and extracted with ethyl acetate (40 mL, 10 mL). The organic layer was dried (MgSO4) and concentrated under reduced pressure. The crude residue was purified by chromatography on silica gel eluting with 0 to 10% ethyl acetate in hexanes to afford the title compound (0.82 g) as a colorless solid.

후처리

  1. customwas obtained
  2. customformed
  3. extractionextracted with ethyl acetate (40 mL, 10 mL)
  4. dry with materialThe organic layer was dried (MgSO4)
  5. concentrationconcentrated under reduced pressure
  6. customThe crude residue was purified by chromatography on silica gel eluting with 0 to 10% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-ac5742b8a8a343139f74ad6f21cb8664
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09302999B2

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