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N-bromobutanimide → HCID 21520278, 화합물

HRID 1282829
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HRID 1282829 반응식
[Br:1]N1C(=O)CCC1=O.[CH2:9]([C:11]1[C:19]2[O:18][C:17]([C:20]3([CH3:25])[O:24][CH2:23][CH2:22][O:21]3)=[CH:16][C:15]=2[CH:14]=[CH:13][CH:12]=1)[CH3:10]>C(Cl)(Cl)(Cl)Cl>[Br:1][CH:9]([C:11]1[C:19]2[O:18][C:17]([C:20]3([CH3:25])[O:24][CH2:23][CH2:22][O:21]3)=[CH:16][C:15]=2[CH:14]=[CH:13][CH:12]=1)[CH3:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 21520276HCID 21520276, 화합물

생성물 1

HCID 21520278HCID 21520278, 화합물

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

반응 조건

온도
0 °C

실험 절차

28.0 g of recrystallized N-bromosuccinimide were added to a solution of 32.5 g of 7-ethyl-2-(2-methyl-1,3-dioxolan-2-yl)benzofuran in 480 ml of carbon tetrachloride. The resulting suspension was stirred and heated under reflux for 12 hours. The mixture was cooled overnight at 0°C, precipitated succinimide was filtered off and the filtrate was evaporated at 30°C under reduced pressure. There was thus obtained crude 7-(1'-bromoethyl)-2-(2-methyl-1,3-dioxolan-2-yl) benzofuran which was used immediately in the next stage. The structure of this compound was confirmed by spectral data.

후처리

  1. temperatureheated
  2. temperatureunder reflux for 12 hours
  3. customprecipitated succinimide
  4. filtrationwas filtered off
  5. customthe filtrate was evaporated at 30°C under reduced pressure

출처 및 근거

ORD 기록
ord-89321039a3d14ea28719b7e82301cda5
출처 데이터셋
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03972900

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