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

HRID 453874
ノート
印刷プレビュー

反応式

HRID 453874 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

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

生成物 1

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

反応条件

温度
25 °C

実験手順

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%

後処理

  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

出典と根拠

ORDレコード
ord-9a0c5dd91536438b8074970b060aef88
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08492559B2

反応ノート

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