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Silicon tetrachloride → 3-Cyano-2,4,5-trifluoro-benzoyl chloride

HRID 49643
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HRID 49643 반응식
[C:1]([C:3]1[C:4]([F:14])=[C:5]([CH:9]=[C:10]([F:13])[C:11]=1[F:12])[C:6](F)=[O:7])#[N:2].[Cl-].[Al+3].[Cl-].[Cl-].[Si](Cl)(Cl)(Cl)[Cl:20]>>[C:1]([C:3]1[C:4]([F:14])=[C:5]([CH:9]=[C:10]([F:13])[C:11]=1[F:12])[C:6]([Cl:20])=[O:7])#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 24816Silicon tetrachlorideHCID 6451240Aluminum(III) ChlorideHCID 153766713-Cyano-2,4,5-trifluoro-benzoyl fluoride

생성물 1

HCID 186187613-Cyano-2,4,5-trifluoro-benzoyl chloride

실험 절차

76.6 g of 3-cyano-2,4,5-trifluoro-benzoyl fluoride were initially introduced together with 1 g of anhydrous aluminium chloride at 60-65° C., and 25 g of silicon tetrachloride were then added dropwise at the rate of gas evolution. After the evolution of gas at 65° C. had ceased, the mixture was distilled under reduced pressure. In the boiling range from 120-122° C./14 mbar, 73.2 g of 3-cyano-2,4,5-trifluoro-benzoyl chloride passed over.

후처리

  1. customat 65° C.
  2. distillationthe mixture was distilled under reduced pressure
  3. customfrom 120-122° C.

출처 및 근거

ORD 기록
ord-2a315c50a0324e4db11b5cd2776cefc3
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706918B2

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