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Sulfuryl chloride → 6-Chloro-7-methoxy-3,4-dihydrocarbostyril

HRID 1979761
ノート
印刷プレビュー

反応式

HRID 1979761 の反応式
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH2:7][CH2:8][C:9](=[O:13])[NH:10]2)=[CH:5][CH:4]=1.S(Cl)([Cl:17])(=O)=O>C(O)(=O)C>[Cl:17][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][C:3]=1[O:2][CH3:1])[NH:10][C:9](=[O:13])[CH2:8][CH2:7]2
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24648Sulfuryl chlorideHCID 128994187-Methoxy-3,4-dihydroquinolin-2(1H)-one

生成物 1

HCID 128994196-Chloro-7-methoxy-3,4-dihydrocarbostyril

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

実験手順

35.4 Grams of 7-methoxy-3,4-dihydrocarbostyril was dissolved in 300 ml of acetic acid and under ice-cooled condition with stirring 27 g of sulfuryl chloride dissolved in 100 ml of acetic acid was added dropwise, then the reaction mixture was allowed to stand overnight. The reaction mixture was poured into 1 liter of ice water and the precipitates were obtained by filtration, washed with water, dried and recrystallized from methanol. 30 Grams of 6-chloro-7-methoxy-3,4-dihydrocarbostyril having the melting point of 212° C. was obtained as in the form of colorless needle-like crystals.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperaturecooled condition
  2. additionwas added dropwise
  3. customthe precipitates were obtained by filtration
  4. washwashed with water
  5. customdried
  6. customrecrystallized from methanol

出典と根拠

ORDレコード
ord-8c907072641e4377a7dc02a4c38b323d
出典データセット
uspto-grants-1984_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04482560

反応ノート

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