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Hydrofluoric Acid → Ethyl 4-methyl-1H-1,2,3-triazole-1-acetate

HRID 887156
ノート
印刷プレビュー

反応式

HRID 887156 の反応式
[CH2:1]([O:3][C:4](=[O:16])[CH2:5][N:6]1[C:10]([Si](C)(C)C)=[C:9]([CH3:15])[N:8]=[N:7]1)[CH3:2].F>C1COCC1.O>[CH2:1]([O:3][C:4](=[O:16])[CH2:5][N:6]1[CH:10]=[C:9]([CH3:15])[N:8]=[N:7]1)[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 14917Hydrofluoric AcidHCID 66839489Ethyl [4-methyl-5-(trimethylsilyl)-1H-1,2,3-triazole-1-yl]acetate

生成物 1

HCID 59603650Ethyl 4-methyl-1H-1,2,3-triazole-1-acetate収率 94.2%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 0.77 g (3.2 mmol) of ethyl [4-methyl-5-(trimethylsilyl)-1H-1,2,3-triazole-1-yl]acetate from step A above in 2 mL of THF was added 1.3 mL (32 mmol) of a solution of 50% hydrofluoric acid in water. The resulting mixture was stirred at room temperature for 3 h and then evaporated to dryness in vacuo. Next, 5 mL of a 2.0 N ammonia in methanol solution was added and then the mixture was again evaporated to dryness in vacuo. The mixture was dissolved in dichloromethane, filtered and then evaporated in vacuo to afford the title compound as a clear gum (0.51 g. 93%). 1HNMR (500 MHz, CDCl3) δ: 7.5 (s, 1H), 5.05 (s, 2H), 4.23 (m, 2H), 2.30 (s, 3H), 1.30 (m, 3H).

後処理

  1. customevaporated to dryness in vacuo
  2. additionNext, 5 mL of a 2.0 N ammonia in methanol solution was added
  3. customthe mixture was again evaporated to dryness in vacuo
  4. dissolutionThe mixture was dissolved in dichloromethane
  5. filtrationfiltered
  6. customevaporated in vacuo

出典と根拠

ORDレコード
ord-dda2b115cdfa47b88fb057d298ca3e12
出典データセット
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08247415B2

反応ノート

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