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4-(1,3-Dioxolan-2-yl)benzonitrile → HCID 22502706、化合物

HRID 1814498
ノート
印刷プレビュー

反応式

HRID 1814498 の反応式
[CH3:1][NH:2][C:3]([C:5]1[CH:9]=[CH:8][S:7][C:6]=1[CH3:10])=[O:4].C([Li])CCC.[O:16]1[CH2:20][CH2:19][O:18][CH:17]1[C:21]1[CH:28]=[CH:27][C:24](C#N)=[CH:23][CH:22]=1>O1CCCC1>[O:16]1[CH2:20][CH2:19][O:18][CH:17]1[C:21]1[CH:28]=[CH:27][C:24]([C:1]2[NH:2][C:3](=[O:4])[C:5]3[CH:9]=[CH:8][S:7][C:6]=3[CH:10]=2)=[CH:23][CH:22]=1
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

5

反応物 3

HCID 27784284-(1,3-Dioxolan-2-yl)benzonitrileHCID 22503091n-Methyl-2-methylthiophene-3-carboxamideHCID 178418339Butyllithium

生成物 1

HCID 22502706HCID 22502706、化合物収率 31.7%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-70 °C

実験手順

To a solution of N-methyl-2-methylthiophene-3-carboxamide (18.5 g) in tetrahydrofuran (350 ml) was dropwise added 2.5M n-butyl lithium (100 ml) at −70° C. The resulting solution was stirred at −70° C. for 1.5 hr, followed by the addition of a solution of 4-(1,3-dioxolan-2-yl)benzonitrile (20.9 g) in tetrahydrofuran (100 ml) at once. After the dry ice/acetone bath was removed, the reaction mixture was back to room temperature. Three hours later, an aqueous solution of saturated ammonium chloride was added thereto, and the organic layer was separated, washed with water and dried. The filtrate was concentrated, and the resulting solid was washed with ethyl acetate, tetrahydrofuran/ether and n-hexane in this order. The resulting solid was then dried, to give the title compound as white crystals (6.24 g, yield; 31.7%).

後処理

  1. customat −70° C
  2. customAfter the dry ice/acetone bath was removed
  3. customwas back to room temperature
  4. additionThree hours later, an aqueous solution of saturated ammonium chloride was added
  5. customthe organic layer was separated
  6. washwashed with water
  7. customdried
  8. concentrationThe filtrate was concentrated
  9. washthe resulting solid was washed with ethyl acetate, tetrahydrofuran/ether and n-hexane in this order
  10. customThe resulting solid was then dried

出典と根拠

ORDレコード
ord-ed283addf68e4cee800a57b569581b75
出典データセット
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06875761B2

反応ノート

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