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(1,1'-Biphenyl)-4-carbonitrile → Hexachloroantimonate

HRID 2273503
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HRID 2273503 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([Br:11])[CH:10]=1)[C:5]([Cl:7])=[O:6].[C:12]1([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:17]=[CH:16][C:15]([C:18]#[N:19])=[CH:14][CH:13]=1.[Sb:26]([Cl:31])([Cl:30])([Cl:29])([Cl:28])[Cl:27]>C(Cl)(Cl)Cl>[C:12]1([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH:13]=[CH:14][C:15]([C:18]2[N:19]=[C:18]([C:15]3[CH:16]=[CH:17][C:12]([C:20]4[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=4)=[CH:13][CH:14]=3)[O+:6]=[C:5]([C:4]3[CH:3]=[C:2]([Br:1])[CH:10]=[C:9]([Br:11])[CH:8]=3)[N:19]=2)=[CH:16][CH:17]=1.[Cl:27][Sb-:26]([Cl:7])([Cl:31])([Cl:30])([Cl:29])[Cl:28]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 18021(1,1'-Biphenyl)-4-carbonitrileHCID 24294Antimony pentachlorideHCID 134505263,5-Dibromobenzoyl chloride

생성물 2

HCID 3695004HexachloroantimonateHCID 866699604,6-Bis(4-biphenylyl)-2-(3,5-dibromophenyl)-1,3,5-oxadiazin-1-ium

시약·촉매·용매 1

HCID 6212
Chloroform
용매

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온도
0 °C

실험 절차

2.98 g of 3,5-dibromobenzoyl chloride and 3.58 g of 4-biphenylcarbonitrile were dissolved in 40 mL of chloroform. The obtained solution was cooled to 0° C., and 2.99 g of antimony pentachloride was added dropwise to the cooled solution. The obtained mixed liquid was stirred at room temperature for 10 minutes, and then, heated under reflux for 14 hours. The obtained reaction mixture was cooled to room temperature, and then distilled under a reduced pressure to remove chloroform to give 4,6-bis(4-biphenylyl)-2-(3,5-dibromophenyl)-1,3,5-oxadiazin-1-ium=hexachloroantimonate as a red solid.

후처리

  1. additionThe obtained mixed liquid
  2. temperatureheated
  3. temperatureunder reflux for 14 hours
  4. customThe obtained reaction mixture
  5. temperaturewas cooled to room temperature
  6. distillationdistilled under a reduced pressure
  7. customto remove chloroform

출처 및 근거

ORD 기록
ord-ba1c038a8b024af0ad4acf8aa9882bb3
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09120773B2

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