Hydrochloric Acid → Methyl methoxy-(4-methoxyphenyl)acetate

HRID 599615노트

반응식

HRID 599615 반응식
C[O-].[Na+].[C:4](O)(=[O:6])C.C(O)(=O)C.IC1C=CC=CC=1.[CH3:19][O:20][C:21]1[CH:26]=[CH:25][C:24]([CH2:27][C:28]([O:30][CH3:31])=[O:29])=[CH:23][CH:22]=1.Cl>CO>[CH3:4][O:6][CH:27]([C:24]1[CH:23]=[CH:22][C:21]([O:20][CH3:19])=[CH:26][CH:25]=1)[C:28]([O:30][CH3:31])=[O:29]

참가 물질

6

실험 절차

A 28% solution of sodium methoxide in methanol (12.8 g) and iodobenzene diacetate (7.15 g) were added to a solution of methyl 4-methoxyphenylacetate (4.0 g) in methanol (60 mL), and the reaction solution was stirred at room temperature for five days. 1 N hydrochloric acid (67 ml) was added dropwise to the reaction solution under ice-cooling, and methanol was evaporated from the reaction solution under reduced pressure. Ethyl acetate was added to the remaining aqueous layer, and the organic layer was separated. The resulting organic layer was sequentially washed with a saturated sodium bicarbonate solution and brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluting solvent: heptane-ethyl acetate system) to obtain 725 mg of the title compound. The property values of the compound are as follows.

후처리

  1. temperaturecooling
  2. custommethanol was evaporated from the reaction solution under reduced pressure
  3. additionEthyl acetate was added to the remaining aqueous layer
  4. customthe organic layer was separated
  5. washThe resulting organic layer was sequentially washed with a saturated sodium bicarbonate solution and brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThe resulting residue was purified by silica gel column chromatography (eluting solvent: heptane-ethyl acetate system)

출처 및 근거

ORD 기록
ord-e58ec8da09cd49e0aa1d169f65f5e68b
출처 데이터셋
uspto-grants-2011_03
특허 번호
US07897632B2

반응 노트

불러오는 중…