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Nitrogen → (E)-2-methyl-3-phenylacrylamide

HRID 2040048
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HRID 2040048 반응식
N#N.[CH3:3]/[C:4](=[CH:8]\[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)/[C:5](O)=[O:6].CC[N:17](CC)CC.ClC(OCC)=O.[NH4+].[OH-]>C1COCC1>[CH3:3]/[C:4](=[CH:8]\[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)/[C:5]([NH2:17])=[O:6]
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참가 물질

7

반응물 5

HCID 947NitrogenHCID 8471TriethylamineHCID 10928Ethyl chloroformateHCID 14923Ammonium HydroxideHCID 637817alpha-Methylcinnamic acid

생성물 1

HCID 6243942(E)-2-methyl-3-phenylacrylamide

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매
2회

반응 조건

온도
0 °C

실험 절차

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of (E)-2-methyl-3-phenylacrylic acid (19.0 g, 116 mmol) and Et3N (17.1 mL, 122 mmol) in THF (500 mL) at 0° C. was treated with ethyl chloroformate (11.4 mL, 117 mmol) and the reaction mixture was stirred at 0° C. for 15 min. A solution of NH4OH (250 mL of a 25% aq. solution) in THF (150 mL) was then added and the reaction mixture was stirred at rt for 90 min. The aq. layer was extracted twice with CH2Cl2 and the combined org. extracts were washed with water, dried over MgSO4, filtered, and the solvents were removed under reduced pressure to give the title compound as a white solid. TLC:rf (1000:50:4 CH2Cl2—MeOH—NH4OH)=0.25

후처리

  1. stirringthe reaction mixture was stirred at rt for 90 min
  2. extractionThe aq. layer was extracted twice with CH2Cl2
  3. washextracts were washed with water
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customthe solvents were removed under reduced pressure

출처 및 근거

ORD 기록
ord-61a4fd177f7f47f193231efab7616262
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08580831B2

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