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O-((4-(trifluoromethyl)phenyl)methyl)hydroxylamine → HCID 118451801, 화합물

HRID 1054221
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인쇄 미리보기

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HRID 1054221 반응식
Cl[C:2]1[N:12]=[CH:11][CH:10]=[CH:9][C:3]=1[C:4]([O:6][CH2:7][CH3:8])=[O:5].[F:13][C:14]([F:25])([F:24])[C:15]1[CH:23]=[CH:22][C:18]([CH2:19][O:20][NH2:21])=[CH:17][CH:16]=1>O>[F:13][C:14]([F:24])([F:25])[C:15]1[CH:23]=[CH:22][C:18]([CH2:19][O:20][NH:21][C:2]2[N:12]=[CH:11][CH:10]=[CH:9][C:3]=2[C:4]([O:6][CH2:7][CH3:8])=[O:5])=[CH:17][CH:16]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2737778O-((4-(trifluoromethyl)phenyl)methyl)hydroxylamineHCID 2796614Ethyl chloronicotinate

생성물 1

HCID 118451801HCID 118451801, 화합물수율 41%

시약·촉매·용매 1

HCID 962Water용매

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온도
120 °C

실험 절차

The mixture of ethyl 2-chloronicotinate (1.4 g, 7.54 mmol) and O-(4-(trifluoromethyl)benzyl)hydroxylamine (2.163 g, 11.31 mmol) was heated at 120° C. for 6 h. Reaction mixture was diluted with water and extracted with EtOAC. The organic layer was separated and distilled out to get crude product which was column purified using 15-20% EtOAc in hexane to get the titled compound in 41% yield.

후처리

  1. customReaction mixture
  2. extractionextracted with EtOAC
  3. customThe organic layer was separated
  4. distillationdistilled out
  5. customto get crude product which
  6. custompurified

출처 및 근거

ORD 기록
ord-5a3defcda2ee4d888cf6b6481f28f1ce
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09394300B2

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