Dimethylformamide → Methyl (3-bromo-4-cyclohexylmethyloxyphenyl)propionate

HRID 2378526노트

반응식

HRID 2378526 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH2:9][CH2:10]C(OC)=O)[CH:5]=[CH:6][C:7]=1[OH:8].[C:15](=[O:18])([O-])[O-:16].[K+].[K+].Br[CH2:22][CH:23]1[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]1.[CH3:29]N(C=O)C>>[Br:1][C:2]1[CH:3]=[C:4]([CH:9]([CH3:10])[C:15]([O:16][CH3:29])=[O:18])[CH:5]=[CH:6][C:7]=1[O:8][CH2:22][CH:23]1[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]1

참가 물질

5

반응물 4

HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 137636Cyclohexane, (bromomethyl)-HCID 22558720Methyl 3-(3-bromo-4-hydroxyphenyl)propanoate

생성물 1

HCID 86614976Methyl (3-bromo-4-cyclohexylmethyloxyphenyl)propionate

실험 절차

A solution of Intermediate 5 (1.29 g) in DMF (25 ml) was added with potassium carbonate (0.86 g) and bromomethylcyclohexane (1.05 ml, TCI), stirred under argon atmosphere at room temperature for 2 hours, then warmed to 60° C., and stirred for 17 hours. The reaction mixture was poured into ice water, and extracted with isopropyl ether (200 ml). The organic layer was successively washed with saturated aqueous sodium hydrogencarbonate, saturated aqueous ammonium chloride, and saturated brine and dried, and then the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography (hexane:isopropyl ether=9:1) to obtain the title compound (Compound No. A-2, 1.45 g).

후처리

  1. temperaturewarmed to 60° C.
  2. stirringstirred for 17 hours
  3. extractionextracted with isopropyl ether (200 ml)
  4. washThe organic layer was successively washed with saturated aqueous sodium hydrogencarbonate, saturated aqueous ammonium chloride, and saturated brine
  5. customdried
  6. customthe solvent was evaporated under reduced pressure
  7. customThe residue was purified by flash column chromatography (hexane:isopropyl ether=9:1)

출처 및 근거

ORD 기록
ord-46956679c45045788f258d3b0e5b951e
출처 데이터셋
uspto-grants-2008_12
특허 번호
US07470807B2

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