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1-(Bromomethyl)-2-chloro-4-iodobenzene → N-[(2-chloro-4-iodophenyl)methyl]phthalimide

HRID 551325
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인쇄 미리보기

반응식

HRID 551325 반응식
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([I:9])=[CH:5][C:4]=1[Cl:10].[C:11]1(=[O:21])[NH:15][C:14](=[O:16])[C:13]2=[CH:17][CH:18]=[CH:19][CH:20]=[C:12]12.[K]>CN(C)C=O.C(OCC)(=O)C>[Cl:10][C:4]1[CH:5]=[C:6]([I:9])[CH:7]=[CH:8][C:3]=1[CH2:2][N:15]1[C:14](=[O:16])[C:13]2=[CH:17][CH:18]=[CH:19][CH:20]=[C:12]2[C:11]1=[O:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 220586831-(Bromomethyl)-2-chloro-4-iodobenzeneHCID 24194345Phthalimide potassium salt

생성물 1

HCID 66719866N-[(2-chloro-4-iodophenyl)methyl]phthalimide수율 72.2%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 8857Ethyl Acetate용매

실험 절차

In a solution of 7.6 g of 1-bromomethyl-2-chloro-4-iodobenzene in 50 mL of N,N-dimethylformamide, 3.7 g of potassium phthalimide was added, and stirred at room temperature for 1 hour. After the completion of the reaction, the reaction mixture was diluted with 80 mL of ethyl acetate, washed with water (30 mL×2), and then dehydrated with and dried over saturated sodium chloride aqueous solution and anhydrous sodium sulfate in that order, and the solvent was distilled off under reduced pressure to obtain 5.7 g of the aimed product as white crystal.

후처리

  1. customAfter the completion of the reaction
  2. washwashed with water (30 mL×2)
  3. dry with materialdried over saturated sodium chloride aqueous solution and anhydrous sodium sulfate in that order
  4. distillationthe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-50478bce35fa47c6a23f3fa2288b7504
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07947715B2

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