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Tetrabutylammonium Fluoride → 1-[4-Hydroxymethyl-1-(2-propenyl)-1H-imidazol-2-yl]ethanone

HRID 242383
ノート
印刷プレビュー

反応式

HRID 242383 の反応式
[Si]([O:18][CH2:19][C:20]1[N:21]=[C:22]([C:28](=[O:30])[CH3:29])[N:23]([CH2:25][CH:26]=[CH2:27])[CH:24]=1)(C(C)(C)C)(C1C=CC=CC=1)C1C=CC=CC=1.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>C1COCC1>[OH:18][CH2:19][C:20]1[N:21]=[C:22]([C:28](=[O:30])[CH3:29])[N:23]([CH2:25][CH:26]=[CH2:27])[CH:24]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 2724141Tetrabutylammonium FluorideHCID 892622101-[4-(tert-Butyldiphenylsilyloxymethyl)-1-(2-propenyl)-1H-imidazol-2-yl]ethanone

生成物 1

HCID 866747321-[4-Hydroxymethyl-1-(2-propenyl)-1H-imidazol-2-yl]ethanone

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

The compound (0.750 g) obtained in (2) was dissolved in THF (50 mL), followed by addition of TBAF (1.0 M THF solution, 1.79 mL) under stirring, and the stirring was continued for 1 hour. The reaction solution was concentrated, and the resulting residue was purified by flash chromatography (ethyl acetate/hexane=5%-÷100%) using amino column (product name: Hi-Flash Column 3 L, manufactured by Yamazen Corporation), washed with ethyl acetate/hexane, and subsequently dried to afford the title compound (0.280 g).

後処理

  1. concentrationThe reaction solution was concentrated
  2. customthe resulting residue was purified by flash chromatography (ethyl acetate/hexane=5%-÷100%)
  3. washwashed with ethyl acetate/hexane
  4. customsubsequently dried

出典と根拠

ORDレコード
ord-c4e4ec8c1b1a4002a63874fea0b7400e
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08653126B2

反応ノート

読み込み中…

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