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Hydrochloric Acid → 2,3-Dimethoxy-benzamidine

HRID 264754
ノート
印刷プレビュー

反応式

HRID 264754 の反応式
C[Si](C)(C)[NH:3][Si](C)(C)C.C([Li])CCC.[CH3:15][O:16][C:17]1[C:24]([O:25][CH3:26])=[CH:23][CH:22]=[CH:21][C:18]=1[C:19]#[N:20].Cl>CCOCC.CCCCCC>[CH3:15][O:16][C:17]1[C:24]([O:25][CH3:26])=[CH:23][CH:22]=[CH:21][C:18]=1[C:19]([NH2:3])=[NH:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 13838HexamethyldisilazaneHCID 218622,3-DimethoxybenzonitrileHCID 178418339Butyllithium

生成物 1

HCID 37009942,3-Dimethoxy-benzamidine

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒
HCID 8058
Hexane
溶媒

実験手順

To a solution of 20 g 1,1,1,3,3,3-hexamethyldisilazane in 150 ml dry ether was added 5 mL 2.4M n-butyllithium in hexane. After 10 min at room temperature, 16.3 g 2,3-dimethoxybenzonitrile was added in one portion and the mixture was kept at room temperature for 16 h. The reaction mixture was then poured onto excess 3N HCl. The aqueous layer was separated, basified with 50% NaOH and the product was extracted three times with 10% methanol in methylene chloride. The combined organic extracts were dried over potassium carbonate and the solvents removed in vacuo to afford 2,3-dimethoxybenzamidine as a glassy solid.

後処理

  1. waitthe mixture was kept at room temperature for 16 h
  2. customThe aqueous layer was separated
  3. extractionthe product was extracted three times with 10% methanol in methylene chloride
  4. dry with materialThe combined organic extracts were dried over potassium carbonate
  5. customthe solvents removed in vacuo

出典と根拠

ORDレコード
ord-d77aed33f0414035a9d400eea285924e
出典データセット
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05646281

反応ノート

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