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Heptylbenzene → 1-Bromo-4-heptylbenzene

HRID 1166022
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HRID 1166022 반응식
[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:14]Br>C(Cl)(Cl)Cl>[Br:14][C:4]1[CH:5]=[CH:6][C:1]([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13])=[CH:2][CH:3]=1
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참가 물질

4

반응물 2

HCID 14115HeptylbenzeneHCID 24408Bromine

생성물 1

HCID 27751001-Bromo-4-heptylbenzene수율 37,921.801%

시약·촉매·용매 1

HCID 6212Chloroform용매

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온도
0 °C

실험 절차

Phenylheptane (100 g, 0.57 mol) was dissolved in 900 mL of chloroform, and ferric chloride (1.41 g, 9 mmol) was added. The mixture was cooled to 0° C. and bromine (32 mL, 0.62 mmol) was added dropwise through an additional funnel. The reaction was kept in dark to prevent the bromination of the aliphatic side chain. After stirring at room temperature overnight, the reaction was quenched with 1N KOH. After extraction, the organic phase was washed with water and dried over MgSO4. The crude product was a brown oil and was purified by column chromatography on silica gel using heptane as an eluent to give 60 g of pure product as light yellow oil at 42% yield. 1H NMR (CDCl3) δ (ppm): 0.88 (t, J=6.9 Hz, 3H), 1.26-1.31 (m, 8H), 1.54-1.59 (m, 2H), 2.54 (t, J=7.8 Hz, 2H), 7.04 (d, J=8.2 Hz, 2H), 7.38 (d, J=8.2 Hz, 2H). FD-MS: m/z 255 (M+).

후처리

  1. customthe reaction was quenched with 1N KOH
  2. extractionAfter extraction
  3. washthe organic phase was washed with water
  4. dry with materialdried over MgSO4
  5. customwas purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-a6d5cc91630245bc8804d18c7cc538b6
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06613457B2

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