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Diisopropylamine → HCID 9907318、化合物

HRID 49958
ノート
印刷プレビュー

反応式

HRID 49958 の反応式
[CH3:1][O:2][C:3]1[CH:13]=[CH:12][C:6]([N:7]([CH3:11])[C:8](=[O:10])[CH3:9])=[CH:5][CH:4]=1.C([N-]C(C)C)(C)C.[Li+].C(NC(C)C)(C)C.C([Li])CCC.[CH2:34]([N:41]1[CH2:46][CH2:45][C:44](=[O:47])[CH2:43][CH2:42]1)[C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1>O.O1CCCC1>[CH3:1][O:2][C:3]1[CH:13]=[CH:12][C:6]([N:7]([CH3:11])[C:8](=[O:10])[CH2:9][C:44]2([OH:47])[CH2:45][CH2:46][N:41]([CH2:34][C:35]3[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=3)[CH2:42][CH2:43]2)=[CH:5][CH:4]=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

8

反応物 5

HCID 7912DiisopropylamineHCID 192201-Benzyl-4-piperidoneHCID 142032Acetamide, N-(4-methoxyphenyl)-N-methyl-HCID 2724682Lithium diisopropylamideHCID 178418339Butyllithium

生成物 1

HCID 9907318HCID 9907318、化合物収率 69.7%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 8028Tetrahydrofuran溶媒3 回

反応条件

温度
-78 °C

実験手順

A solution of 4′-methoxy-N-methylacetanilide (12 g) in an anhydrous tetrahydrofuran (30 mL) was added to a solution in an anhydrous tetrahydrofuran (100 mL) of lithium diisopropylamide prepared from diisopropylamine (10.5 mL) and n-butyl lithium (1.53M hexane solution; 48 mL) at below −65° C., and the mixture was stirred at −78° C. for 15 minutes. An anhydrous tetrahydrofuran solution (20 mL) of 1-benzylpiperidin-4-one (12.7 g) was then added to this reaction mixture at below −65° C., and the resulting mixture was stirred at −78° C. for 10 minutes. After increasing the temperature to room temperature, water was added to the mixture, and the mixed solution was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried over anhydrous sodium sulfate, followed by distilling off the solvent under reduced pressure. The residue obtained was recrystallized from ether-hexane to obtain the titled compound (17.2 g).

後処理

  1. stirringthe resulting mixture was stirred at −78° C. for 10 minutes
  2. temperatureAfter increasing the temperature to room temperature
  3. extractionthe mixed solution was extracted with ethyl acetate
  4. washThe organic layer was washed with water and saturated brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. distillationby distilling off the solvent under reduced pressure
  7. customThe residue obtained
  8. customwas recrystallized from ether-hexane

出典と根拠

ORDレコード
ord-7da2c7e3439d4fd09da343e794317901
出典データセット
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06710060B2

反応ノート

読み込み中…

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