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Acetic Anhydride → HCID 15740989, 화합물

HRID 1529820
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HRID 1529820 반응식
[Br:1][C:2]1[S:3][C:4]([Br:10])=[CH:5][C:6]=1[N+:7]([O-])=O.[C:11](OC(=O)C)(=[O:13])[CH3:12]>[Fe]>[Br:1][C:2]1[S:3][C:4]([Br:10])=[CH:5][C:6]=1[NH:7][C:11](=[O:13])[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 49618952,5-Dibromo-3-nitrothiophene

생성물 1

HCID 15740989HCID 15740989, 화합물수율 58%

시약·촉매·용매 1

HCID 23925Iron촉매

실험 절차

To an ice cold solution of 2,5-dibromo-3-nitrothiophene (5.0 g, 17.4 mmol, DellErba, C.; Spinelli, D. Tetrahedron, 1965, 21, 1061-1066) in acetic acid-acetic anhydride (1:1, 50 mL) was added iron powder (5.8 g, 104.5 mmol) slowly for 15 min. and stirred at rt for 4 h. After completion of the reaction, the reaction mixture was poured into ice cold water (500 mL) and stirred for 15 min. The precipitated solid was filtered, washed with water and dried. The crude product was chromatographed over silica gel column using hexane-EtOAc (95:5) as eluent to give the product as a white color solid (3.0 g, 58%), mp 114-116° C. 1H NMR (400 MHz, CDCl3): δ 7.78 (1H, s), 7.21 (1H, s), 2.20 (3H, s).

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후처리

  1. customAfter completion of the reaction
  2. stirringstirred for 15 min
  3. filtrationThe precipitated solid was filtered
  4. washwashed with water
  5. customdried
  6. customThe crude product was chromatographed over silica gel column

출처 및 근거

ORD 기록
ord-8c40ac65906143bdbd3b9b55b6c22384
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09090633B2

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