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Hydrazine hydrate (1:1) → HCID 23301566, 화합물

HRID 376891
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HRID 376891 반응식
C1([C:4]([C:13]([C:15]([CH:24]2[CH2:26]C2)=CC2C=CC=C(O)C=2)=O)=[CH:5][C:6]2[CH:11]=[CH:10][CH:9]=[C:8]([OH:12])[CH:7]=2)CC1.O.[NH2:28][NH2:29]>O>[CH:15]1([C:13]2[CH2:4][CH:5]([C:6]3[CH:11]=[CH:10][CH:9]=[C:8]([OH:12])[CH:7]=3)[NH:29][N:28]=2)[CH2:24][CH2:26]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 86755112HCID 86755112, 화합물

생성물 1

HCID 23301566HCID 23301566, 화합물수율 67.6%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

To a 500 ml round bottom flask equipped with magnetic stirrer and reflux condenser was charged 13.2 g (0.0702 moles) of cyclopropyl 3-hydroxystyrylketone 150 mls of water and 3.5 g (0.0702 moles) of hydrazine monohydrate. The reaction was refluxed for a total of 2 hours, after which it was cooled and diluted with an additional 200 mls of water. The resulting solid was collected by vacuum filtration, washed with water and hexane, and dried in vacuuo at 40° C. overnight to afford 9.6 g of 3-cyclopropyl-5-(3-hydroxyphenyl)-2-pyrazoline as a tan solid at a 68% isolated yield.

후처리

  1. customTo a 500 ml round bottom flask equipped with magnetic stirrer
  2. temperaturereflux condenser
  3. temperatureThe reaction was refluxed for a total of 2 hours
  4. temperatureafter which it was cooled
  5. filtrationThe resulting solid was collected by vacuum filtration
  6. washwashed with water and hexane
  7. customdried in vacuuo at 40° C. overnight

출처 및 근거

ORD 기록
ord-d97cec0078d24317bb85341cc3f93d54
출처 데이터셋
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06022891

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