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Ammonia → 6-Chloro-3,4-dihydroisoquinolin-1(2H)-one

HRID 2277582
ノート
印刷プレビュー

反応式

HRID 2277582 の反応式
C[O:2][C:3](=O)[NH:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([Cl:13])[CH:8]=1.N>>[Cl:13][C:9]1[CH:8]=[C:7]2[C:12](=[CH:11][CH:10]=1)[C:3](=[O:2])[NH:4][CH2:5][CH2:6]2
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 222AmmoniaHCID 897069HCID 897069、化合物

生成物 1

HCID 193756376-Chloro-3,4-dihydroisoquinolin-1(2H)-one収率 39.1%

反応条件

温度
120 °C

実験手順

Under N2 protection, a mixture of [2-(3-chloro-phenyl)-ethyl]-carbamic acid methyl ester (5.0 g, 23.4 mmol) and PPA (polyphosphoric acid) (20 g) in a 250 mL round-bottom flask was vigorously stirred at 120° C. for 2 hours. After cooling to room temperature, the reaction mixture was treated with ice-water and aqueous ammonia solution to adjust the pH to 8. Then, the mixture was then extracted with EtOAc, and the organic layer was washed with brine, dried over anhy. Na2SO4 and filtered. After removal of solvent under reduced pressure, the crude product obtained was further washed with ethyl ether to give title compound (1.66 g, 39%) as a white solid. MS: 182.0 (M+H+).

後処理

  1. temperatureAfter cooling to room temperature
  2. extractionThen, the mixture was then extracted with EtOAc
  3. washthe organic layer was washed with brine
  4. customdried over anhy
  5. filtrationNa2SO4 and filtered
  6. customAfter removal of solvent under reduced pressure
  7. customthe crude product obtained
  8. washwas further washed with ethyl ether

出典と根拠

ORDレコード
ord-30778ba399ee41ed9caf598fbed29c9d
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09133158B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート