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HCID 18477136、化合物 → HCID 18477085、化合物

HRID 2188202
ノート
印刷プレビュー

反応式

HRID 2188202 の反応式
[CH2:1]([CH2:8][NH:9][CH2:10][CH:11]1[CH2:20][CH2:19][C:18]2[C:13](=[CH:14][CH:15]=[C:16]([F:21])[CH:17]=2)[C:12]1([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>FC(F)(F)C(O)=O>[CH2:1]([CH2:8][NH:9][CH2:10][C:11]1[CH2:20][CH2:19][C:18]2[C:13](=[CH:14][CH:15]=[C:16]([F:21])[CH:17]=2)[C:12]=1[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 18477136HCID 18477136、化合物

生成物 1

HCID 18477085HCID 18477085、化合物収率 67.9%

試薬・触媒・溶媒 1

HCID 6422Trifluoroacetic acid溶媒

実験手順

Trifluoroacetic acid (10 cm3) was added to 2-(N-benzylmethylamino)methyl-6-fluoro-1-phenyl-1,2,3,4-tetrahydronaphthalene-1-ol (1.5 g) and the resulting solution was stirred at room temperature for 2 h. The excess trifluoroacetic acid was removed under reduced pressure and the resultant brown oil was taken up into petroleum ether (b. p. 40-60° C.) and passed through a short column [basic alumina, eluting with petroleum ether (b. p. 40-60° C.)-ethyl acetate (20:1)]. The fractions containing the product were combined and the solvent removed under reduced pressure to afford the title compound (0.97 g).

後処理

  1. customThe excess trifluoroacetic acid was removed under reduced pressure
  • washpassed through a short column [basic alumina, eluting with petroleum ether (b. p. 40-60° C.)-ethyl acetate (20:1)]
  • additionThe fractions containing the product
  • customthe solvent removed under reduced pressure
  • 出典と根拠

    ORDレコード
    ord-ed0dccf687b1477cafc10da447d4253e
    出典データセット
    uspto-grants-2002_06
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06410592B1

    反応ノート

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