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

HRID 2297623
ノート
印刷プレビュー

反応式

HRID 2297623 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8857Ethyl AcetateHCID 21956813HCID 21956813、化合物HCID 178418546HCID 178418546、化合物

生成物 1

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

試薬・触媒・溶媒 1

HCID 13387N-methyl-2-pyrrolidone溶媒

実験手順

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).

後処理

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

出典と根拠

ORDレコード
ord-f41c9bdbd5ad4eb3925b37850c6e1242
出典データセット
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06492378B1

反応ノート

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