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Cyclopropylamine → CID 74043826

HRID 2073816
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인쇄 미리보기

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HRID 2073816 반응식
[F:1][C:2]1[C:19]([F:20])=[C:18]([F:21])[C:17]([F:22])=[C:16]([CH3:23])[C:3]=1[C:4]([C:6](=[CH:12]OCC)[C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:5].[CH:24]1([NH2:27])[CH2:26][CH2:25]1>C(O)C>[F:1][C:2]1[C:19]([F:20])=[C:18]([F:21])[C:17]([F:22])=[C:16]([CH3:23])[C:3]=1[C:4]([C:6](=[CH:12][NH:27][CH:24]1[CH2:26][CH2:25]1)[C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 69828CyclopropylamineHCID 54293321Ethyl 2-(2-methyl-3,4,5,6-tetrafluorobenzoyl)3-ethoxyacrylate

생성물 1

HCID 178471859CID 74043826수율 97.3%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
5 °C

실험 절차

To a solution of 9.0 g (27.0 mmol) of ethyl 2-(2,3,4,5-tetrafluoro-6-methylbenzoyl)-3-ethoxyacrylate in 30 ml of absolute ethanol at 5° C. was added 1.68 g (29.4 mmol) of cyclopropylamine. The mixture was stirred at 5° C. for 1.5 hours and at room temperature for 2.5 hours. The solution was concentrated to an oil which was triturated with hexane to give a tan solid. The crude product was recrystallized from hexane to give 9.07 g of the title compound, mp 72°-74° C.

후처리

  1. concentrationThe solution was concentrated to an oil which
  2. customwas triturated with hexane
  3. customto give a tan solid
  4. customThe crude product was recrystallized from hexane

출처 및 근거

ORD 기록
ord-3ba8195a7c444845817d801c32bfaa60
출처 데이터셋
uspto-grants-1990_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04920120

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