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O-Toluidine → N-(2-Methylphenyl)pyrrolidine

HRID 1925739
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HRID 1925739 반응식
[NH2:1][C:2]1[C:3]([CH3:8])=[CH:4][CH:5]=[CH:6][CH:7]=1.C(=O)([O-])[O-].[Na+].[Na+].Br[CH2:16][CH2:17][CH2:18][CH2:19]Br>CO.O>[C:3]1([CH3:8])[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[N:1]1[CH2:19][CH2:18][CH2:17][CH2:16]1
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참가 물질

6

반응물 3

HCID 7242O-ToluidineHCID 80561,4-DibromobutaneHCID 10340Sodium Carbonate

생성물 1

HCID 142531N-(2-Methylphenyl)pyrrolidine수율 41.1%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

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온도
50 °C

실험 절차

To a solution of o-toluidine (2.0 g; 18.7 mmol) in methanol (62 mL) was added sodium carbonate (4.95 g; 46.75 mmol) followed by 1,4-dibromobutane (4.85 g; 22.4 mmol). The resulting mixture was stirred at 50° C. under a nitrogen atmosphere overnight and then diluted with water and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The crude residue was purified by automated silica gel column chromatography (Biotage®) eluting with ethyl acetate/hexanes (0 to 40% v/v over 900 mL gradient elution) to yield the title product as a dark yellow-orange oil (1.24 g).

후처리

  1. extractionextracted with ethyl acetate
  2. dry with materialThe organic layer was dried over magnesium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. customThe crude residue was purified by automated silica gel column chromatography (Biotage®)
  6. washeluting with ethyl acetate/hexanes (0 to 40% v/v over 900 mL gradient elution)

출처 및 근거

ORD 기록
ord-90640e867e4f4781b5da5988b85986ff
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08178699B2

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