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Azido(trimethyl)stannane → 5-(2-Bromo-4-chloro-6-fluoro-phenyl)-2H-tetrazole

HRID 2046569
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인쇄 미리보기

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HRID 2046569 반응식
[Br:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[C:6]([F:11])[C:3]=1[C:4]#[N:5].[N:12]([Sn](C)(C)C)=[N+:13]=[N-:14]>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[C:6]([F:11])[C:3]=1[C:4]1[N:12]=[N:13][NH:14][N:5]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5104973Azido(trimethyl)stannaneHCID 585795372-Bromo-4-chloro-6-fluorobenzonitrile

생성물 1

HCID 679792895-(2-Bromo-4-chloro-6-fluoro-phenyl)-2H-tetrazole수율 88.7%

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
120 °C

실험 절차

A mixture of 2-bromo-4-chloro-6-fluoro-benzonitrile (4 g, 17.06 mmol) and azidotrimethyltin (3.86 g, 18.77 mmol) in toluene (100 ml) was heated to 120° C. for 72 h. After completion of the reaction, the mixture was partitioned between EtOAc (50 ml) and aqueous 0.5N HCl solution (40 ml). The organic layer was separated, washed with water and brine, dried with Na2SO4 and concentrated under reduced pressure to afford the title compound (4.2 g, 87%) as red solid.

후처리

  1. customAfter completion of the reaction
  2. customthe mixture was partitioned between EtOAc (50 ml) and aqueous 0.5N HCl solution (40 ml)
  3. customThe organic layer was separated
  4. washwashed with water and brine
  5. dry with materialdried with Na2SO4
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-894b472c4021436c95b35f1bcbdda3d0
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08592426B2

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