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Water → Ethyl 1-phenyl-1H-1,2,3-triazole-4-carboxylate

HRID 1177927
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반응식

HRID 1177927 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:8]([O:10][C:11](=[O:17])[C:12](=[N+:15]=[N-:16])[CH:13]=O)[CH3:9].O>CCO>[CH2:8]([O:10][C:11]([C:12]1[N:15]=[N:16][N:1]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH:13]=1)=[O:17])[CH3:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 6115AnilineHCID 54182403Ethyl 2-diazo-2-formylacetate

생성물 1

HCID 5270623Ethyl 1-phenyl-1H-1,2,3-triazole-4-carboxylate수율 87.41%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Aniline (143 mg, 1.5 mmol) was added to a solution of 2-diazo-3-oxo-propionic acid ethyl ester (200 mg, 1.4 mmol) and HAc (0.2 mL) in EtOH (0.5 mL) and stirring was at room temperature overnight. Reaction mixture was concentrated to get the residue. Cold water was then added, filtered the solid precipitated to afford 264 mg (87.41% Yield) of 1-phenyl-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester. 1H NMR (CDCl3): δ 8.5 (s, 1H), 7.8 (d, 2H), 7.6-7.48 (m, 3H), 4.5 (q, 2H), 1.4 (t, 3H).

후처리

  1. customReaction mixture
  2. concentrationwas concentrated
  3. customto get the residue
  4. filtrationfiltered the solid
  5. customprecipitated

출처 및 근거

ORD 기록
ord-98a15cba1383432390b8d331548503f0
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07842696B2

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