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Ethyl Acetate → Methyl 2-methoxy-5-cyano-4-iso-propylbenzoate

HRID 2187540
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HRID 2187540 반응식
[Cu][C:2]#[N:3].[CH3:4][O:5][C:6]1[CH:15]=[C:14]([CH:16]([CH3:18])[CH3:17])[C:13](Br)=[CH:12][C:7]=1[C:8]([O:10][CH3:11])=[O:9].C(OCC)(=O)C>CN1CCCC1=O>[CH3:4][O:5][C:6]1[CH:15]=[C:14]([CH:16]([CH3:18])[CH3:17])[C:13]([C:2]#[N:3])=[CH:12][C:7]=1[C:8]([O:10][CH3:11])=[O:9]
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참가 물질

5

반응물 3

HCID 8857Ethyl AcetateHCID 21956813HCID 21956813, 화합물HCID 178418546HCID 178418546, 화합물

생성물 1

HCID 21956833Methyl 2-methoxy-5-cyano-4-iso-propylbenzoate수율 74.8%

시약·촉매·용매 1

HCID 13387N-methyl-2-pyrrolidone용매

실험 절차

Copper (I) cyanide (550 mg, 6 mmol) was added to a solution of methyl 2-methoxy-5-bromo-4-iso-propylbenzoate (861 mg) in N-methyl-2-pyrolidinone (30 ml). The mixture was stirred under argon and boiled under reflux for 4 h. The mixture was cooled, poured into excess ice/water and ethyl acetate and filtered. The organic phase was separated, washed with water, brine and dried(MgSO4). Evaporation gave a crude brown solid which was purified by chromatography on silica gel eluting with ethyl acetate/n-hexane (1:4). The product was obtained as a white solid (523 mg).

후처리

  1. temperatureunder reflux for 4 h
  2. temperatureThe mixture was cooled
  3. filtrationfiltered
  4. customThe organic phase was separated
  5. washwashed with water, brine and dried(MgSO4)
  6. customEvaporation
  7. customgave a crude brown solid which
  8. customwas purified by chromatography on silica gel eluting with ethyl acetate/n-hexane (1:4)

출처 및 근거

ORD 기록
ord-d576ffc2d6004e8f90419dc4ecc379d0
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06410555B1

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