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Dimethyl Sulfoxide → 5-Nitro-2-(2,2,2-trifluoroethoxy)pyridine

HRID 46465
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HRID 46465 반응식
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=1.[F:11][C:12]([F:16])([F:15])[CH2:13][OH:14].[OH-].[Li+].CS(C)=O>O>[F:11][C:12]([F:16])([F:15])[CH2:13][O:14][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 679Dimethyl SulfoxideHCID 3939Lithium HydroxideHCID 64092,2,2-TrifluoroethanolHCID 783082-Chloro-5-nitropyridine

생성물 1

HCID 6137185-Nitro-2-(2,2,2-trifluoroethoxy)pyridine

시약·촉매·용매 1

HCID 962Water용매

실험 절차

2-Chloro-5-nitropyridine (9.5 grams), 2,2,2-trifluoroethanol (6.0 grams), and lithium hydroxide (4.0 grams) were mixed in 50 ml. of DMSO and stirred overnight (about 18 hours) at room temperature. The reaction mixture was then poured into water and the product was separated by filtration. It was crystallized from ethyl acetate-hexanes, yield 5.0 grams, m.p., 35°-37° C.

후처리

  1. customthe product was separated by filtration
  2. customIt was crystallized from ethyl acetate-hexanes, yield 5.0 grams
  3. custom35°-37° C.

출처 및 근거

ORD 기록
ord-558bb867ab5c4bd4a3b4e2b03e7cc939
출처 데이터셋
uspto-grants-1979_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04173639

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