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Isoamyl Nitrite → 3-Methyl-4-(trifluoromethyl)benzonitrile

HRID 268910
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HRID 268910 반응식
N[C:2]1[CH:9]=[C:8]([C:10]([F:13])([F:12])[F:11])[C:7]([CH3:14])=[CH:6][C:3]=1[C:4]#[N:5].N(OCCC(C)C)=O>C1COCC1.CC(OC)(C)C>[CH3:14][C:7]1[CH:6]=[C:3]([CH:2]=[CH:9][C:8]=1[C:10]([F:11])([F:12])[F:13])[C:4]#[N:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 8053Isoamyl Nitrite2회HCID 53416444HCID 53416444, 화합물

생성물 1

HCID 574686963-Methyl-4-(trifluoromethyl)benzonitrile

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 15413tert-Butyl methyl ether용매

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온도
23 °C

실험 절차

To a solution of 2-amino-5-methyl-4-trifluoromethyl-benzonitrile from step 4 (23.34 g, 117 mmol) in dry THF (350 mL) was added isoamyl nitrite (34.3 mL, 257 mmol), and the mixture was refluxed for 20 h. Additional isoamyl nitrite (16.6 mL, 129 mmol) was added and the mixture was refluxed for further 20 h. The mixture was cooled to 23° C. and diluted with TBME, the organic layer was washed with 1 N HCl, sat. NaHCO3-sol. and brine, dried over Na2SO4.

후처리

  1. temperaturethe mixture was refluxed for 20 h
  2. temperaturethe mixture was refluxed for further 20 h
  3. washthe organic layer was washed with 1 N HCl, sat. NaHCO3-sol
  4. dry with materialand brine, dried over Na2SO4

출처 및 근거

ORD 기록
ord-46697044b81f4e88bf8c20af30d17f25
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07446113B2

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