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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N-bromobutanimide → 2-(Bromomethyl)-4-(trifluoromethyl)furan

HRID 1654112
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HRID 1654112 반응식
[CH3:1][C:2]1[O:3][CH:4]=[C:5]([C:7]([F:10])([F:9])[F:8])[CH:6]=1.[Br:11]N1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl.N(C(C)(C)C#N)=NC(C)(C)C#N>[Br:11][CH2:1][C:2]1[O:3][CH:4]=[C:5]([C:7]([F:10])([F:9])[F:8])[CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 67184N-bromobutanimideHCID 218197502-Methyl-4-(trifluoromethyl)furan

생성물 1

HCID 218197532-(Bromomethyl)-4-(trifluoromethyl)furan수율 60.1%

시약·촉매·용매 2

HCID 6547Azobisisobutyronitrile촉매HCID 5943Carbon Tetrachloride용매

실험 절차

6 g of the product of Stage D were refluxed for 1 and a half hours in 50 ml of carbon tetrachloride in the presence of 7.2 g of N-bromosuccinimide and 0.3 g of azobisisobutyronitrile and the mixture was allowed to return to room temperature and was filtered. The solvent was evaporated and the residue was chromatographed on silica (eluent: 98/2 ether/isopropyl ether) to obtain 5.5 g of the expected product.

후처리

  1. customto return to room temperature
  2. filtrationwas filtered
  3. customThe solvent was evaporated
  4. customthe residue was chromatographed on silica (eluent: 98/2 ether/isopropyl ether)

출처 및 근거

ORD 기록
ord-b3d89a00b8414e9d93c3bacac0ffbde1
출처 데이터셋
uspto-grants-1995_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05405865

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