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Bromine → 6-Bromo-3,4-dihydro-4-methyl-2(1H)-quinolinone

HRID 986017
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반응식

HRID 986017 반응식
[Br:1]Br.[CH3:3][CH:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][C:6](=[O:14])[CH2:5]1>C(O)(=O)C>[Br:1][C:11]1[CH:12]=[C:13]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:14])[CH2:5][CH:4]2[CH3:3]
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참가 물질

4

반응물 2

HCID 24408BromineHCID 52461484-methyl-3,4-dihydro-1H-quinolin-2-one

생성물 1

HCID 201589746-Bromo-3,4-dihydro-4-methyl-2(1H)-quinolinone

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

실험 절차

A solution of bromine (0.08 cm3) in acetic acid (1 cm3) was added at room temperature to a stirred solution of 4-methyl-3,4-dihydro-2-(1H)-quinolone (0.5 g) in acetic acid (4.0 cm3). After 2 hours, volatile material was removed in vacuo, the residue was partitioned between chloroform (50 cm3) and water (20 cm3), and the organic phase was further extracted with chloroform (2×20 cm3). The combined and dried (MgSO4) organic extracts were evaporated in vacuo and the solid residue was recrystallised from ethyl acetate to afford 6-bromo-4-methyl-3,4-dihydro-2-(1H)-quinolone, m.p. 190°, (0.35 g).

후처리

  1. customvolatile material was removed in vacuo
  2. customthe residue was partitioned between chloroform (50 cm3) and water (20 cm3)
  3. extractionthe organic phase was further extracted with chloroform (2×20 cm3)
  4. dry with materialdried (MgSO4) organic extracts
  5. customwere evaporated in vacuo
  6. customthe solid residue was recrystallised from ethyl acetate

출처 및 근거

ORD 기록
ord-7553d1d884034a6e93dc5b31500d4c53
출처 데이터셋
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04710507

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