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Hydrochloric Acid → 2,3-Dimethoxy-benzamidine

HRID 277710
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HRID 277710 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

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

생성물 1

HCID 37009942,3-Dimethoxy-benzamidine

시약·촉매·용매 2

HCID 3283Diethyl Ether용매
HCID 8058
Hexane
용매

실험 절차

To a solution of 20 g 1,1,1,3,3,3-hexamethyldisilazane in 150 mL dry ether was added 5 mL 2.4 M 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.

후처리

  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

출처 및 근거

ORD 기록
ord-64b326563c7d4e46be270d71e125295e
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06358955B1

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