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Water → HCID 86692457、化合物

HRID 1748507
ノート
印刷プレビュー

反応式

HRID 1748507 の反応式
[O:1]1[C:5]2([CH2:10][CH2:9][CH:8]([C:11]#[N:12])[CH2:7][CH2:6]2)[O:4][CH2:3][CH2:2]1.C[Si]([N-][Si](C)(C)C)(C)C.[Li+].[Br:23][C:24]1[CH:25]=[CH:26][C:27](F)=[N:28][CH:29]=1.O>O1CCCC1>[Br:23][C:24]1[CH:25]=[CH:26][C:27]([C:8]2([C:11]#[N:12])[CH2:9][CH2:10][C:5]3([O:4][CH2:3][CH2:2][O:1]3)[CH2:6][CH2:7]2)=[N:28][CH:29]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 2733832Lithium hexamethyldisilazaneHCID 27831685-Bromo-2-fluoropyridineHCID 111164331,4-Dioxaspiro[4.5]decane-8-carbonitrile

生成物 1

HCID 86692457HCID 86692457、化合物収率 68.7%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒
2 回

実験手順

After 1,4-dioxaspiro[4,5]decane-8-carbonitrile (2.5 g) was dissolved in tetrahydrofuran (8 ml), 1M tetrahydrofuran-solution of lithium bis(trimethylsilyl)amide (15 ml) was added at 0° C. and stirred for 30 minutes. 5-Bromo-2-fluoropyridine (2.64 g) was further added and stirred at room temperature for two hours. Water was added to the reaction solution, extracted with ethyl acetate and concentrated in vacuo. The residue was purified with silica gel chromatography (n-hexane/ethyl acetate) and the resulting solid was washed with n-hexane to give the titled compound (3.32 g).

後処理

  1. stirringstirred at room temperature for two hours
  2. extractionextracted with ethyl acetate
  3. concentrationconcentrated in vacuo
  4. customThe residue was purified with silica gel chromatography (n-hexane/ethyl acetate)
  5. washthe resulting solid was washed with n-hexane

出典と根拠

ORDレコード
ord-0c40b9f34c89422fb2684c4ca45a3b4a
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09150555B2

反応ノート

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