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Hydrazine → HCID 178438050, 화합물

HRID 403501
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HRID 403501 반응식
[C:1]([CH:3]([C:13](=O)[CH2:14][CH3:15])[CH2:4][C:5]1[CH:12]=[CH:11][C:8]([C:9]#[N:10])=[CH:7][CH:6]=1)#[N:2].[NH2:17][NH2:18]>CCO>[NH2:2][C:1]1[NH:18][N:17]=[C:13]([CH2:14][CH3:15])[C:3]=1[CH2:4][C:5]1[CH:12]=[CH:11][C:8]([C:9]#[N:10])=[CH:7][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9321HydrazineHCID 683790834-(2-Cyano-3-oxopentyl)benzonitrile

생성물 1

HCID 178438050HCID 178438050, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a 500 ml, four-necked flask equipped with an overhead stirrer, a thermocouple and a condenser was charged 4-(2-cyano-3-oxopentyl)benzonitrile (25) (5 g, 23.6 mmol) and 50 ml of EtOH. The solution was stirred and hydrazine (1.65 g, 33 mmol, 64%, 1.4 eq) was added. The batch was stirred at 65° C. for 3 hours. The solvent was concentrated by vacuum and the residue was slurried with 50 ml of MTBE at room temperature for 30 min. The precipitate was collected by vacuum filtration and the solid was washed with MTBE to give product 26 as a white solid.

후처리

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  1. customTo a 500 ml, four-necked flask equipped with an overhead stirrer
  2. stirringThe batch was stirred at 65° C. for 3 hours
  3. concentrationThe solvent was concentrated by vacuum
  4. filtrationThe precipitate was collected by vacuum filtration
  5. washthe solid was washed with MTBE

출처 및 근거

ORD 기록
ord-fdfd190df9244ea499b38dbd97d901e3
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08748435B2

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