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Water → 5-Nitro-2-(piperazin-1-yl)benzonitrile

HRID 2184855
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HRID 2184855 반응식
Cl[C:2]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][C:3]=1[C:4]#[N:5].[NH:13]1[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1.O>COCCO>[C:4]([C:3]1[CH:6]=[C:7]([N+:10]([O-:12])=[O:11])[CH:8]=[CH:9][C:2]=1[N:13]1[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1)#[N:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 4837PiperazineHCID 855042-Chloro-5-nitrobenzonitrile

생성물 1

HCID 167682915-Nitro-2-(piperazin-1-yl)benzonitrile수율 99.8%

시약·촉매·용매 1

HCID 80192-Methoxyethanol용매

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온도
60 °C

실험 절차

A mixture of 2-chloro-5-nitrobenzonitrile (1 g) and piperazine (2.12 g) in ethylene glycol monomethyl ether (5 mL) was heated at 60° C. for 30 minutes. After cooling to room temperature, H2O was added (50 mL) and the solution extracted with CH2Cl2 (3×25 mL). The combined organic layers were washed with H2O, dried over Na2SO4 and evaporated to dryness to give 1.27 g (99%) of the desired compound.

후처리

  1. temperatureAfter cooling to room temperature
  2. extractionthe solution extracted with CH2Cl2 (3×25 mL)
  3. washThe combined organic layers were washed with H2O
  4. dry with materialdried over Na2SO4
  5. customevaporated to dryness

출처 및 근거

ORD 기록
ord-5cc7a83edf3c40e59f8afa3cba7e7001
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06399614B1

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