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Ethyl Acrylate → HCID 43365416, 화합물

HRID 1985085
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HRID 1985085 반응식
[CH2:1]([C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[CH:5][CH:4]=1)[CH3:2].[C:10]([O:14][CH2:15][CH3:16])(=[O:13])[CH:11]=[CH2:12].[OH-].[Na+]>C(O)(=O)C>[CH2:1]([C:3]1[CH:9]=[CH:8][C:6]([NH:7][CH2:12][CH2:11][C:10]([O:14][CH2:15][CH3:16])=[O:13])=[CH:5][CH:4]=1)[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8821Ethyl Acrylate2회HCID 115044-EthylanilineHCID 14798Sodium Hydroxide

생성물 1

HCID 43365416HCID 43365416, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
80 °C

실험 절차

To a solution of 4-ethyl aniline (10.0 g) in acetic acid (25 mL) was added ethyl acrylate (10.8 g). The mixture was heated to 80° C. for 2 hours. Additional ethyl acrylate (1.0 mL) was added, and the mixture was again heated to 80° C. for 1 hour. The mixture was allowed to cool to room temperature and stir for two days. Sodium hydroxide (8N) was added until the pH equaled 9. The mixture was partitioned between dichloromethane and water and the combined organics were washed once with 1N sodium hydroxide, once with brine, dried with sodium sulfate, filtered, and concentrated. The mixture was chromatographed using a 20% ethyl acetate in heptane solvent solution. A mixture of the mono and di ester product (19.5 g) were obtained (1:1 mixture). MS (ESI+) for C13H19NO2 m/z 221.99 (M+H)+.

후처리

  1. temperaturethe mixture was again heated to 80° C. for 1 hour
  2. temperatureto cool to room temperature
  3. customThe mixture was partitioned between dichloromethane and water
  4. washthe combined organics were washed once with 1N sodium hydroxide, once with brine
  5. dry with materialdried with sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe mixture was chromatographed
  9. additionA mixture of the mono and di ester product (19.5 g)
  10. customwere obtained (1:1 mixture)

출처 및 근거

ORD 기록
ord-d438d866ad1a48539169c8d1b35e98ba
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07544717B2

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