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Methanol → Methyl 3-bromo-5-ethylbenzoate

HRID 1397262
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HRID 1397262 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([CH2:11][CH3:12])[CH:10]=1)[C:5]([OH:7])=[O:6].O=S(Cl)Cl.[CH3:17]O>>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([CH2:11][CH3:12])[CH:10]=1)[C:5]([O:7][CH3:17])=[O:6]
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참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 8260993-Bromo-5-ethylbenzoic acid

생성물 1

HCID 67325611Methyl 3-bromo-5-ethylbenzoate수율 92%

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온도
0 °C

실험 절차

The compound 3-bromo-5-ethylbenzoic acid (0.95 g, 4.14 mmol) was dissolved in MeOH (50 mL), reaction mixture was cooled to 0° C. and SOCl2 (0.5 mL) was added. The reaction mixture was allowed to stir at room temperature for 10 h. The reaction mixture was concentrated under reduced pressure and diluted with CH2Cl2. The organic layer was washed with 10% NaHCO3 solution, water and brine. The organic phase was dried over anhydrous sodium sulfate and solvent was removed under reduced pressure. Methyl 3-bromo-5-ethylbenzoate (0.92 g, yield 92%) was isolated as colorless liquid and carried through without further purification. 1H NMR (300 MHz, CDCl3) δ 7.99 (t, J=1.6 Hz, 1H), 7.81 (d, J=1.4 Hz, 1H), 7.54 (t, J=1.6 Hz, 1H), 3.92 (s, 3H), 2.69 (q, J=7.6 Hz, 2H), 1.26 (t, J=7.6 Hz, 3H).

후처리

  1. customreaction mixture
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. additiondiluted with CH2Cl2
  4. washThe organic layer was washed with 10% NaHCO3 solution, water and brine
  5. dry with materialThe organic phase was dried over anhydrous sodium sulfate and solvent
  6. customwas removed under reduced pressure

출처 및 근거

ORD 기록
ord-4fde1fafff39434ab3c31fa7bdefa708
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08901156B2

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