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

HRID 887156
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HRID 887156 반응식
[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]
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참가 물질

5

반응물 2

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

생성물 1

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

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-dda2b115cdfa47b88fb057d298ca3e12
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08247415B2

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