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

HRID 623689
ノート
印刷プレビュー

反応式

HRID 623689 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 5360545SodiumHCID 10942334Sodium MethoxideHCID 901113321-Methoxy-4-methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazolium tetrafluoroborate2 回

生成物 1

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

試薬・触媒・溶媒 2

HCID 887Methanol溶媒
HCID 962
Water
溶媒

反応条件

温度
23 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-ac5742b8a8a343139f74ad6f21cb8664
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09302999B2

反応ノート

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