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Bromine → Methyl 4-bromoacetyl-2,6-dichlorophenoxyacetate

HRID 266734
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HRID 266734 반응식
[Br:1]Br.[C:3]([C:6]1[CH:17]=[C:16]([Cl:18])[C:9]([O:10][CH2:11][C:12]([O:14][CH3:15])=[O:13])=[C:8]([Cl:19])[CH:7]=1)(=[O:5])[CH3:4]>C(Cl)(Cl)Cl>[Br:1][CH2:4][C:3]([C:6]1[CH:7]=[C:8]([Cl:19])[C:9]([O:10][CH2:11][C:12]([O:14][CH3:15])=[O:13])=[C:16]([Cl:18])[CH:17]=1)=[O:5]
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참가 물질

4

반응물 2

HCID 24408BromineHCID 18918381Methyl 4-acetyl-2,6-dichlorophenoxyacetate

생성물 1

HCID 18918498Methyl 4-bromoacetyl-2,6-dichlorophenoxyacetate

시약·촉매·용매 1

HCID 6212Chloroform용매2회

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온도
40 °C

실험 절차

A solution of bromine (0.77 ml) in chloroform (10 ml) was added dropwise over 15 minutes to a stirred solution of the product from step (i) (4.16 g) in chloroform (40 ml) at 25° C. The temperature was raised to 40° C. for 1 hour and then stirring continued for a further 18 hours at ambient temperature. The solvent was removed in vacuo and the residual oil purified by flash chromatography on silica, eluting with dichloromethane, to give a crystalline solid. Recrystallisation from methanol gave methyl 4-bromoacetyl-2,6-dichlorophenoxyacetate, 1.88 g, as white crystals: m.p. 89°-90° C.; NMR (d6DMSO) δ 8.06 (2H, s), 4.93 (2H, s), 4.82 (2H, s), 3.72 (3H, s); m/e 355/357 (M+H)+, 1Br pattern; calculated for C11H9BrCl2O4 : C, 37.1; H, 2.3. found: C, 36.8; H, 2.4%.

후처리

  1. customThe solvent was removed in vacuo
  2. customthe residual oil purified by flash chromatography on silica
  3. washeluting with dichloromethane
  4. customto give a crystalline solid
  5. customRecrystallisation from methanol

출처 및 근거

ORD 기록
ord-f303d78ed8a94fcbab8f8ff0ac9c5dac
출처 데이터셋
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05652242

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