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1,3-Benzodioxol-5-amine → Methyl 4-[3-[N-(3,4-methylenedioxyphenyl)amino]propoxy]benzoate

HRID 359079
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HRID 359079 반응식
[CH2:1]1[O:10][C:9]2[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][C:3]=2[O:2]1.Cl[CH2:12][CH2:13][CH2:14][O:15][C:16]1[CH:25]=[CH:24][C:19]([C:20]([O:22][CH3:23])=[O:21])=[CH:18][CH:17]=1.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[CH2:1]1[O:10][C:9]2[CH:8]=[CH:7][C:5]([NH:6][CH2:12][CH2:13][CH2:14][O:15][C:16]3[CH:25]=[CH:24][C:19]([C:20]([O:22][CH3:23])=[O:21])=[CH:18][CH:17]=3)=[CH:4][C:3]=2[O:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 843101,3-Benzodioxol-5-amineHCID 516892Sodium BicarbonateHCID 12389265Methyl 4-(3-chloropropoxy)benzoate

생성물 1

HCID 14882821Methyl 4-[3-[N-(3,4-methylenedioxyphenyl)amino]propoxy]benzoate수율 75.3%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

3,4-Methylenedioxyaniline (1.80 g), methyl 4-(3chloropropoxy)benzoate (2.0 g) and sodium bicarbonate (1.47 g) in toluene (20 ml) were heated with stirring under refluxing for 29 hours. The reaction solution was concentrated under reduced pressure, and thereto were added water and an equivalent amount of conc. hydrochloric acid, then, the resulting precipitate was collected by filtration. After washed with water, the precipitate was recrystallized from aqueous methanol to give the desired product (2.17 g). mp. 124°-127° C.

후처리

  1. temperatureunder refluxing for 29 hours
  2. concentrationThe reaction solution was concentrated under reduced pressure
  3. additionwere added water
  4. filtrationan equivalent amount of conc. hydrochloric acid, then, the resulting precipitate was collected by filtration
  5. washAfter washed with water
  6. customthe precipitate was recrystallized from aqueous methanol

출처 및 근거

ORD 기록
ord-d87afd5a21a143158153228a379058e9
출처 데이터셋
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04999378

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