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Methanol → Methyl 3-chloro-1H-pyrrole-2-carboxylate

HRID 453874
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HRID 453874 반응식
[Cl:1][C:2]1(Cl)[C:6]([C:7](Cl)(Cl)Cl)=[N:5][CH2:4][CH2:3]1.[CH3:12][O-:13].[Na+].C[OH:16]>>[Cl:1][C:2]1[CH:3]=[CH:4][NH:5][C:6]=1[C:7]([O:13][CH3:12])=[O:16]
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참가 물질

4

반응물 3

HCID 887MethanolHCID 10942334Sodium MethoxideHCID 216737514,4-Dichloro-5-(trichloromethyl)-3,4-dihydro-2H-pyrrole

생성물 1

HCID 5324605Methyl 3-chloro-1H-pyrrole-2-carboxylate수율 83%

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온도
25 °C

실험 절차

4,4-Dichloro-5-(trichloromethyl)-3,4-dihydro-2H-pyrrole (47.4 mmol, 1.0 equiv.) was added to a solution of sodium methanolate (284.5 mmol, 6.0 equiv.) in methanol (126 ml), and the mixture was heated for 1.5 h at boiling temperature. The reaction mixture was cooled to 25° C., the solvent was concentrated under reduced pressure, the residue was taken up in diethyl ether (470 ml), and the mixture was stirred for 30 min. The resulting solid (sodium chloride) was filtered out, and the filtrate was dried over K2CO3 and concentrated under reduced pressure. The residue was taken up in DCM (600 ml), extracted with 2 N HCl (2×150 ml), dried over Na2SO4 and concentrated under reduced pressure. The crude product was used in the next step without being purified further. Yield: 83%

후처리

  1. temperaturethe mixture was heated for 1.5 h
  2. concentrationthe solvent was concentrated under reduced pressure
  3. filtrationThe resulting solid (sodium chloride) was filtered out
  4. dry with materialthe filtrate was dried over K2CO3
  5. concentrationconcentrated under reduced pressure
  6. extractionextracted with 2 N HCl (2×150 ml)
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated under reduced pressure
  9. customwithout being purified further

출처 및 근거

ORD 기록
ord-9a0c5dd91536438b8074970b060aef88
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08492559B2

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