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Methanol → Methyl 2-bromo-4-methoxybenzoate

HRID 1471348
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HRID 1471348 반응식
O=S(Cl)Cl.[Br:5][C:6]1[CH:14]=[C:13]([O:15][CH3:16])[CH:12]=[CH:11][C:7]=1[C:8]([OH:10])=[O:9].[CH3:17]O>O>[Br:5][C:6]1[CH:14]=[C:13]([O:15][CH3:16])[CH:12]=[CH:11][C:7]=1[C:8]([O:10][CH3:17])=[O:9]
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참가 물질

5

반응물 3

HCID 887Methanol2회HCID 24386Thionyl Chloride2회HCID 144847132-Bromo-4-methoxybenzoic acid

생성물 1

HCID 15110997Methyl 2-bromo-4-methoxybenzoate수율 85%

시약·촉매·용매 1

HCID 962Water용매

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온도
79 °C

실험 절차

SOCl2 (7.5 mL, 103.0 mmol) is added dropwise to a stirred 0° C. suspension of 2-bromo-4-methoxybenzoic acid (3) (6.5 g, 28.1 mmol) in methanol (12 mL). The mixture is next stirred at 79° C. for 18 h and then cooled to room temperature before removal of methanol and excess SOCl2 at reduced pressure. The residue is diluted with H2O (50 mL) and extracted with ethyl acetate (100 mL and 70 mL). The extract is washed (2 N NaOH and brine) and dried. After solvent removal at reduced pressure, the residue is purified on silica gel (14.3% to 16.7% ethyl acetate/hexane) to give 5.9 g (85%) of 4 as a colorless liquid. IR 2952, 1728, 1597, 1261 cm−1; 1H NMR (CDCl3) δ 3.83 (s, 3H, CH3O), 3.89 (s, 3H, CO2CH3), 6.86 (dd, J=7.2, 2.0 Hz, 1H, 5-PhH), 7.18 (d, J=2.0 Hz, 1H, 3-PhH), 7.85 ppm (d, J=7.2 Hz, 1H, 6-PhH).

후처리

  1. extractionextracted with ethyl acetate (100 mL and 70 mL)
  2. washThe extract is washed (2 N NaOH and brine)
  3. customdried
  4. customAfter solvent removal at reduced pressure
  5. customthe residue is purified on silica gel (14.3% to 16.7% ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-764c725f7f144c22ad483420dd343eec
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09012217B2

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