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Acetic Anhydride → 6-Bromo-1H-indole-3-carbonitrile

HRID 1618636
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HRID 1618636 반응식
[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([CH:11]=O)=[CH:7][NH:8]2)=[CH:4][CH:3]=1.[NH2:13]O.Cl.CC(OC(C)=O)=O>N1C=CC=CC=1>[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([C:11]#[N:13])=[CH:7][NH:8]2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7918Acetic AnhydrideHCID 443297Hydroxyamine hydrochlorideHCID 27948306-Bromoindole-3-carbaldehyde

생성물 1

HCID 114700676-Bromo-1H-indole-3-carbonitrile

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To a solution of 6-bromo-1H-indole-3-carbaldehyde (1.2 g, 5.36 mmol) in pyridine (10 mL) was added NH2OH.HCl (0.424 g, 6.11 mmol) portionwise and the resulting mixture was stirred at rt for 1.5 h. 25 mL of Ac2O was added and the mixture was heated at reflux overnight. After this time the reaction mixture was cooled to rt and poured into ice. The resulting solid was filtered and the product was purified by flash column chromatography to give 6-bromo-1H-indole-3-carbonitrile slightly impure but was used for the next step. Mass Spectrum (ESI) m/e=222 (M+1).

후처리

  1. temperaturethe mixture was heated
  2. temperatureat reflux overnight
  3. temperatureAfter this time the reaction mixture was cooled to rt
  4. additionpoured into ice
  5. filtrationThe resulting solid was filtered
  6. customthe product was purified by flash column chromatography

출처 및 근거

ORD 기록
ord-1249dd06b51c4028ab2e8e0879b64549
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08765940B2

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