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Hexachloroethane → Tert-butyl 5-chloro-2,4-difluoronicotinate

HRID 1481776
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HRID 1481776 반응식
[Li+].CC([N-]C(C)C)C.[F:9][C:10]1[N:22]=[CH:21][CH:20]=[C:19]([F:23])[C:11]=1[C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13].[Cl:24]C(Cl)(Cl)C(Cl)(Cl)Cl>C1COCC1>[Cl:24][C:20]1[CH:21]=[N:22][C:10]([F:9])=[C:11]([C:19]=1[F:23])[C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13]
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참가 물질

5

반응물 3

HCID 6214HexachloroethaneHCID 2724682Lithium diisopropylamideHCID 71281946Tert-butyl 2,4-difluoronicotinate

생성물 1

HCID 71281897Tert-butyl 5-chloro-2,4-difluoronicotinate수율 48.1%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매3회

실험 절차

Into a solution of LDA in THF (20 mL, 12 mmol) was added a solution of tert-butyl 2,4-difluoronicotinate (2.14 g, 10 mmol) in THF (12 mL) at −78° C. The mixture was stirred for 30 min and then a solution of hexachloroethane (2.96 g, 12.5 mmol) in THF (7.0 mL) was added. The temperature was allowed to rise to 0° C. The reaction was then quenched with saturated NH4Cl. The mixture was extracted with ethyl acetate and the organic layers were combined, dried over sodium sulfate, evaporated and purified by silica chromatography (0-8% ethyl acetate in hexanes) to give tert-butyl 5-chloro-2,4-difluoronicotinate (1.2 g, 48%).

후처리

  1. customto rise to 0° C
  2. customThe reaction was then quenched with saturated NH4Cl
  3. extractionThe mixture was extracted with ethyl acetate
  4. dry with materialdried over sodium sulfate
  5. customevaporated
  6. custompurified by silica chromatography (0-8% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-88a20d163dd5466797e222ab737558cc
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409905B2

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