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2-Thiophenecarboxaldehyde → Ethyl 2-azido-3-(2-thienyl)propenoate

HRID 1017728
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HRID 1017728 반응식
[N:1]([CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6])=[N+:2]=[N-:3].[S:10]1[CH:14]=[CH:13][CH:12]=[C:11]1[CH:15]=O.[O-]CC.[K+].[Cl-].[NH4+]>C(O)C>[N:1]([C:4](=[CH:15][C:11]1[S:10][CH:14]=[CH:13][CH:12]=1)[C:5]([O:7][CH2:8][CH3:9])=[O:6])=[N+:2]=[N-:3]
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참가 물질

6

반응물 4

HCID 73642-ThiophenecarboxaldehydeHCID 25517Ammonium ChlorideHCID 69480Acetic acid, azido-, ethyl esterHCID 23670592Potassium ethoxide

생성물 1

HCID 54362140Ethyl 2-azido-3-(2-thienyl)propenoate수율 25%

시약·촉매·용매 1

HCID 702Ethanol용매
2회

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온도
0 °C

실험 절차

A solution of ethyl azidoacetate (1.38 g) and thiophene-2-carboxaldehyde (1 g) in ethanol (20 ml) was added dropwise to a solution of potassium ethoxide (0.9 g) in ethanol (20 ml) at 0° C. The reaction was stirred for 2 hours at 0° C. and 2 hours at ambient temperature then poured into saturated aqueous ammonium chloride solution (150 ml) and extracted with ether. Combined organic extracts were dried (MgSO4), concentrated in vacuo and the residue purified by column chromatography using isohexane as eluent to give the product as a pale yellow crystalline solid (0.49 g, 25%), NMR d(CDCl3) 1.40 (3H, t), 4.37 (2H, q), 7.08 (2H, m), 7.18 (1H, s), 7.38 (1H, m), 7.52 (1H, d).

후처리

  1. extractionextracted with ether
  2. dry with materialCombined organic extracts were dried (MgSO4)
  3. concentrationconcentrated in vacuo
  4. customthe residue purified by column chromatography

출처 및 근거

ORD 기록
ord-080d2bc859cf421d8a886680a13be622
출처 데이터셋
uspto-grants-2002_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06479527B1

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