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Tetrabutylammonium Fluoride Trihydrate → HCID 17874146、化合物

HRID 1890494
ノート
印刷プレビュー

反応式

HRID 1890494 の反応式
[Si]([O:8][CH2:9][C:10]1[CH:15]=[CH:14][N:13]=[C:12]([NH:16][CH3:17])[N:11]=1)(C(C)(C)C)(C)C.O.O.O.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1>[OH:8][CH2:9][C:10]1[CH:15]=[CH:14][N:13]=[C:12]([NH:16][CH3:17])[N:11]=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 11726816Tetrabutylammonium Fluoride TrihydrateHCID 57971147HCID 57971147、化合物

生成物 1

HCID 17874146HCID 17874146、化合物収率 269.5%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

4-tert-Butyldimethylsilyloxymethyl-2-methylaminopyrimidine (40 mg, 0.16 mmol, Reference Compound No. 6-1) was dissolved in tetrahydrofuran (3.0 mL), then a solution of tetrabutylammonium fluoride trihydrate (55 mg, 0.17 mmol) in tetrahydrofuran (3.0 mL) was added thereto, and the mixture was stirred for 40 minutes at room temperature. The reaction mixture was concentrated under reduced pressure. The residue was suspended into 25% methanol-chloroform solution, and the mixture was filtered with silica gel (2.0 g). The filtrate was concentrated under reduced pressure to give 60 mg of the mixture of the title Reference Compound and tetrabutylammonium fluoride as a brown oil.

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. filtrationthe mixture was filtered with silica gel (2.0 g)
  3. concentrationThe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-4747b4a832f9415a8c721181bef68643
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08507485B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート