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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Tert-Butylamine → N-(tert-butyl)-3,5,6-trifluoropyridin-2-amine

HRID 368392
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인쇄 미리보기

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HRID 368392 반응식
F[C:2]1[C:7]([F:8])=[CH:6][C:5]([F:9])=[C:4]([F:10])[N:3]=1.[C:11]([NH2:15])([CH3:14])([CH3:13])[CH3:12]>C(#N)C>[C:11]([NH:15][C:2]1[C:7]([F:8])=[CH:6][C:5]([F:9])=[C:4]([F:10])[N:3]=1)([CH3:14])([CH3:13])[CH3:12]
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참가 물질

4

반응물 2

HCID 6385Tert-ButylamineHCID 1377492,3,5,6-Tetrafluoropyridine

생성물 1

HCID 22121202N-(tert-butyl)-3,5,6-trifluoropyridin-2-amine수율 65.2%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
60 °C

실험 절차

To 40 ml of acetonitrile were added 11.0 g of 2,3,5,6-tetrafluoropyridine and 18.5 g of t-butylamine, and the mixture was stirred at 60° C. for 3 days, and the solvent and the like were distilled off. To the residue was added 100 ml of chloroform, and the mixture was washed with 50 ml of distilled water. The chloroform layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 9.7 g of the title compound as a pale yellow oil.

후처리

  1. distillationthe solvent and the like were distilled off
  2. additionTo the residue was added 100 ml of chloroform
  3. washthe mixture was washed with 50 ml of distilled water
  4. dry with materialThe chloroform layer was dried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-412fdec089a94f62bfaf9731103381c6
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06133284

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