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Benzaldehyde → Styryl[4-(4-fluorophenyl)piperazino] sulfone

HRID 1582050
ノート
印刷プレビュー

反応式

HRID 1582050 の反応式
[Li+].CC([N-]C(C)C)C.C([Li])CCC.C(NC(C)C)(C)C.[F:21][C:22]1[CH:27]=[CH:26][C:25]([N:28]2[CH2:33][CH2:32][N:31]([S:34]([CH3:37])(=[O:36])=[O:35])[CH2:30][CH2:29]2)=[CH:24][CH:23]=1.C(OP(Cl)(OCC)=O)C.[CH:47](=O)[C:48]1[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=1>C1COCC1>[F:21][C:22]1[CH:23]=[CH:24][C:25]([N:28]2[CH2:33][CH2:32][N:31]([S:34](/[CH:37]=[CH:47]/[C:48]3[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=3)(=[O:35])=[O:36])[CH2:30][CH2:29]2)=[CH:26][CH:27]=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 6

HCID 240BenzaldehydeHCID 7912DiisopropylamineHCID 13139Diethyl chlorophosphateHCID 6690391-(4-Fluorophenyl)-4-(methylsulfonyl)piperazineHCID 2724682Lithium diisopropylamideHCID 178418339Butyllithium

生成物 1

HCID 882266
Styryl[4-(4-fluorophenyl)piperazino] sulfone
収率 46.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒4 回

反応条件

温度
-78 °C

実験手順

To a solution of LDA [8.5 mmol ; prepared by slow addition of n-butyl lithium (3.5 ml, 8.5 mmol, 2.5 M in hexane) to a solution of diisopropylamine (860 mg, 8.5 mmol) in dry THF (5 ml) at −78° C.] at −78° C. was added a solution of 1-(4-fluorophenyl)4-(methanesulfonyl)piperazine (1 g, 3.87 mmol) in THF (25 ml) dropwise. The mixture was stirred at −78° C. for 1 hour and a solution of diethylchlorophosphate (670 mg; 3.87 mmol) in THF (3 ml) was added. The mixture was stirred at −78° C. for 1 hour and benzaldehyde (450 mg; 4.24 mmol) in THF (3 ml) was added. The mixture was gently warmed to room temperature and stirred for 18 hours. The mixture was washed with aqueous ammonium chloride and extracted with ethyl acetate. The organic layers were washed with water, brine and dried over MgSO4. Purification of the residue on silica (eluant: dichloromethane) afforded 1-(4-fluorophenyl)4(trans-β-styrenesulfonyl)piperazine as a white powder (621 mg, 46%).

後処理

  1. stirringThe mixture was stirred at −78° C. for 1 hour
  2. temperatureThe mixture was gently warmed to room temperature
  3. stirringstirred for 18 hours
  4. washThe mixture was washed with aqueous ammonium chloride
  5. extractionextracted with ethyl acetate
  6. washThe organic layers were washed with water, brine
  7. dry with materialdried over MgSO4
  8. customPurification of the residue on silica (eluant: dichloromethane)

出典と根拠

ORDレコード
ord-af3bcab8828840e69b146a71e8189780
出典データセット
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06734184B1

反応ノート

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