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Trifluoroacetic acid → 4-(Azetidin-3-yloxy)pyridine

HRID 2171683
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HRID 2171683 반응식
[N:1]1[CH:6]=[CH:5][C:4]([O:7][CH:8]2[CH2:11][N:10](C(OC(C)(C)C)=O)[CH2:9]2)=[CH:3][CH:2]=1.C(O)(C(F)(F)F)=O>ClCCCl>[NH:10]1[CH2:11][CH:8]([O:7][C:4]2[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=2)[CH2:9]1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 24902675Tert-butyl 3-(pyridin-4-yloxy)azetidine-1-carboxylate

생성물 1

HCID 509882824-(Azetidin-3-yloxy)pyridine수율 90.4%

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

tert-Butyl 3-(pyridin-4-yloxy)azetidine-1-carboxylate (494 mg) was mixed with DCE (5 ml), and TFA (2 ml) was added thereto, followed by stirring at room temperature for 5 hours. The reaction mixture was concentrated under reduced pressure, and the obtained residue was purified by basic silica gel column chromatography (CHCl3/MeOH) to obtain 4-(azetidin-3-yloxy)pyridine (268 mg).

후처리

  1. additionwas added
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. customthe obtained residue was purified by basic silica gel column chromatography (CHCl3/MeOH)

출처 및 근거

ORD 기록
ord-df85a70c7d7544fe8f6d05a1f75d664d
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09051283B2

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