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Bromine → Methyl 4-bromo-7-methoxy-2H-1,3-benzodioxole-5-carboxylate

HRID 258153
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인쇄 미리보기

반응식

HRID 258153 반응식
[CH3:1][O:2][C:3]1[C:4]2[O:15][CH2:14][O:13][C:5]=2[CH:6]=[C:7]([CH:12]=1)[C:8]([O:10][CH3:11])=[O:9].[Br:16]Br>C(O)(=O)C>[Br:16][C:6]1[C:5]2[O:13][CH2:14][O:15][C:4]=2[C:3]([O:2][CH3:1])=[CH:12][C:7]=1[C:8]([O:10][CH3:11])=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24408BromineHCID 601780Methyl 3,4-methylenedioxy-5-methoxybenzoate

생성물 1

HCID 11449108Methyl 4-bromo-7-methoxy-2H-1,3-benzodioxole-5-carboxylate수율 51%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

In 35 ml of acetic acid was dissolved 10.5 g of methyl 5-methoxy-3,4-methylenedioxybenzoate, and a solution of bromine (formed by diluting 8 g of bromine with 25 ml of acetic acid) was dropped into the solution over a period of 1 hour. The mixture was stirred at room temperature for 10 hours and the reaction liquid was poured into ice water, and the formed precipitate was recovered by filtration and recrystallized from ethanol to obtain methyl 2-bromo-5-methoxy-3,4-methylenedioxybenzoate (the yield was 51%).

후처리

  1. customthe reaction liquid
  2. filtrationthe formed precipitate was recovered by filtration
  3. customrecrystallized from ethanol

출처 및 근거

ORD 기록
ord-721af72956c94556ae745bc4f58863fa
출처 데이터셋
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05264594

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