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Chlorotrimethylsilane → Methyl 2-(2-methylquinolin-8-yl)acetate

HRID 338903
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HRID 338903 반응식
[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[C:5]([CH2:12][C:13]([OH:15])=[O:14])[CH:6]=[CH:7][CH:8]=2)[N:3]=1.Cl[Si](C)(C)[CH3:18]>CO>[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[C:5]([CH2:12][C:13]([O:15][CH3:18])=[O:14])[CH:6]=[CH:7][CH:8]=2)[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6397ChlorotrimethylsilaneHCID 70984126HCID 70984126, 화합물

생성물 1

HCID 70984092Methyl 2-(2-methylquinolin-8-yl)acetate수율 87%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 2-(2-methylquinolin-8-yl)acetic acid (1.45 g, 7.21 mmol) in dry MeOH (100 mL) was added chlorotrimethylsilane (1.82 mL, 14.4 mmol) dropwise at 0° C. After addition, the reaction mixture was stirred at reflux for 2 hours. After cooling to ambient temperature, the solvent was removed under reduced pressure. The residue was partitioned between ethyl acetate (50 mL) and saturated sodium bicarbonate (20 mL). The organic layer was separated, washed with brine, dried (sodium sulfate), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (5:1 hexane/ethyl acetate) to give methyl 2-(2-methylquinolin-8-yl)acetate (1.35 g, 87.0%) as an oil.

후처리

  1. additionAfter addition
  2. temperatureat reflux for 2 hours
  3. customthe solvent was removed under reduced pressure
  4. customThe residue was partitioned between ethyl acetate (50 mL) and saturated sodium bicarbonate (20 mL)
  5. customThe organic layer was separated
  6. washwashed with brine
  7. dry with materialdried (sodium sulfate)
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe residue was purified by flash chromatography on silica gel (5:1 hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-02cb02e808b2400fbda5e3ac2bee9edd
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889704B2

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