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Anisole → 4-Bromo-4'-methoxybenzophenone

HRID 750052
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HRID 750052 반응식
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](Cl)=[O:7])=[CH:4][CH:3]=1.[Al+3].[Cl-].[Cl-].[Cl-].[CH3:15][O:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>[N+](C1C=CC=CC=1)([O-])=O>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([C:20]2[CH:21]=[CH:22][C:17]([O:16][CH3:15])=[CH:18][CH:19]=2)=[O:7])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7519AnisoleHCID 685154-Bromobenzoyl chlorideHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 7943334-Bromo-4'-methoxybenzophenone수율 94.8%

시약·촉매·용매 1

HCID 7416Nitrobenzene용매2회

실험 절차

To a solution of 4-bromo-benzoyl chloride (3.3 g, 15 mmol) and AlCl3 (2.6 g, 20 mmol) in nitrobenzene (20 mL) was added a solution of methoxy-benzene (1.5 g, 14.5 mmol) in nitrobenzene (5 mL) slowly at 0° C. The resulting mixture was allowed to warm to rt and stir at rt for 16 h. The mixture was poured onto 150 mL ice-water solution and extracted with CH2Cl2 (5×100 mL). The combined organic layers were washed with water (2×100 mL) and brine (50 mL). and dried over anhy. Na2SO4. The solvent was removed in vacuo to obtain the crude product which was purified by recrystallization from cyclohexane to yield the title product (4.0 g, 91%) as a solid; 1H NMR (500 MHz, CDCl3); δ 3.90 (s, 3H), 6.97 (d, J=8.5, 2H), 7.63 (d, J=2.0, 4H), 7.79 (d, J=9.0, 2H).

후처리

  1. extractionextracted with CH2Cl2 (5×100 mL)
  2. washThe combined organic layers were washed with water (2×100 mL) and brine (50 mL)
  3. customand dried over anhy
  4. customThe solvent was removed in vacuo
  5. customto obtain the crude product which
  6. customwas purified by recrystallization from cyclohexane

출처 및 근거

ORD 기록
ord-dcd0a86d7a764c75846d1b64edff917b
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07402684B2

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