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Calcium Carbonate → 3-((3-Hydroxypropyl)methylamino)benzonitrile

HRID 591141
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HRID 591141 반응식
[CH3:1][NH:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[C:6]#[N:7].Cl[CH2:12][CH2:13][CH2:14][OH:15].C([O-])([O-])=O.[Ca+2]>O>[OH:15][CH2:14][CH2:13][CH2:12][N:2]([CH3:1])[C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[C:6]#[N:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10112Calcium CarbonateHCID 123133-Chloro-1-propanolHCID 177940363-(Methylamino)benzonitrile

생성물 1

HCID 617014023-((3-Hydroxypropyl)methylamino)benzonitrile수율 125.7%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

3-methylaminobenzonitrile (17.34 g, 0.13 mol, 1.0 eq), 3-chloropropanol (49.70 g, 0.53 mol, 4.0 eq) and CaCO3 (52.50 g, 0.53 mol, 4.0 eq) are added into water (230 ml) at room temperature, the mixture is refluxed at elevated temperature for 40 h, and cooled, filtered and extracted with ethyl acetate (200 ml*3). The organic phases are combined, washed with water (100 ml*2), washed with saturated brine twice, dried over anhydrous sodium sulfate and concentrated to give a light yellow oily crude product (31.08 g). The residue could be used directly in next step without purification.

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후처리

  1. temperaturethe mixture is refluxed at elevated temperature for 40 h
  2. temperaturecooled
  3. filtrationfiltered
  4. extractionextracted with ethyl acetate (200 ml*3)
  5. washwashed with water (100 ml*2)
  6. washwashed with saturated brine twice
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-1723ece1455f45aba67d49edc065cfe3
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09238632B2

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