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Benzoyl chloride, 3-bromo- → HCID 25054619, 화합물

HRID 391502
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인쇄 미리보기

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HRID 391502 반응식
N1N[N:3]=[N:4][C:5]=1[C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1.[Br:12][C:13]1[CH:14]=[C:15]([CH:19]=[CH:20][CH:21]=1)[C:16](Cl)=[O:17]>CC1C=CC=CC=1C>[Br:12][C:13]1[CH:14]=[C:15]([C:16]2[O:17][C:5]([C:6]3[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=3)=[N:4][N:3]=2)[CH:19]=[CH:20][CH:21]=1
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참가 물질

4

반응물 2

HCID 74377Benzoyl chloride, 3-bromo-HCID 1510915-(3-Pyridyl)tetrazole

생성물 1

HCID 25054619HCID 25054619, 화합물

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

16.8 g (114 mmol) of 3-(2H-tetrazol-5-yl)pyridine) according to Synthesis Example 7 and 25 g (114 mmol) of 3-bromobenzoylchloride were dissolved in 180 mL of o-xylene. The solution was reacted at 150° C. for 8 hours. The acquired reactant was purified under reduced pressure and washed with methanol, obtaining 30 g (Y=87%) of a white solid.

후처리

  1. customThe solution was reacted at 150° C. for 8 hours
  2. customThe acquired reactant was purified under reduced pressure
  3. washwashed with methanol
  4. customobtaining 30 g (Y=87%) of a white solid

출처 및 근거

ORD 기록
ord-69451d115958415b9c722df003378e15
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08383932B2

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