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Methyltriphenylphosphonium chloride → HCID 178435233、化合物

HRID 480155
ノート
印刷プレビュー

反応式

HRID 480155 の反応式
[Cl-].[CH3:2][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Li]CCCC.[O:27]=[C:28]1[N:36]([CH2:37][CH2:38][CH3:39])[C:35]2[NH:34][C:33]([C:40]34[CH2:47][CH2:46][C:43]([CH:48]=O)([CH2:44][CH2:45]3)[CH2:42][CH2:41]4)=[N:32][C:31]=2[C:30](=[O:50])[N:29]1[CH2:51][CH2:52][CH3:53]>C1COCC1>[CH2:51]([N:29]1[C:30](=[O:50])[C:31]2[N:32]=[C:33]([C:40]34[CH2:47][CH2:46][C:43]([CH:48]=[CH2:2])([CH2:44][CH2:45]3)[CH2:42][CH2:41]4)[NH:34][C:35]=2[N:36]([CH2:37][CH2:38][CH3:39])[C:28]1=[O:27])[CH2:52][CH3:53]
参加物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 9879809Methyltriphenylphosphonium chlorideHCID 178418339ButyllithiumHCID 178456486HCID 178456486、化合物

生成物 1

HCID 178435233HCID 178435233、化合物収率 38%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a stirred suspension of methyl triphenylphosphonium chloride (1.07 g, 3.0 mmol) in THF (20 ml) at 0° C. was added n-BuLi (1.4 M in hexane, 2.14 ml, 3.0 mmol). The resulting reddish-brown mixture was stirred at this temperature for 0.5 h and then at rt for 0.5 h. A solution of 4-(2,6-dioxo-1,3-dipropyl-2,3,6,9-tetrahydro-1H-purin-8-yl)-bicyclo[2.2.2]octane-1-carbaldehyde (372 mg, 1.0 mmol) in THF (10 ml) was added over a period of 20 minutes and the resulting mixture was stirred overnight (12 h). The reaction mixture was partitioned between saturated aqeuous NH4Cl (20 ml) and EtOAc (20 ml) and the aqueous phase was extracted with EtOAc (20 ml). The combined organic extracts were washed with saturated aqeuous NaCl (50 ml), dried (MgSO4), filtered and evaporated in vacuo to afford an oil that was purified by radial chromatography (2 mm plate) using a gradient of 0-5% MeOH in CH2Cl2 as eluent. Product-containing fractions were combined and concentrated to afford 140 mg (38%) of a white solid. MS: 371 (MH+).

後処理

  1. waitat rt for 0.5 h
  2. stirringthe resulting mixture was stirred overnight (12 h)
  3. customThe reaction mixture was partitioned between saturated aqeuous NH4Cl (20 ml) and EtOAc (20 ml)
  4. extractionthe aqueous phase was extracted with EtOAc (20 ml)
  5. washThe combined organic extracts were washed with saturated aqeuous NaCl (50 ml)
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customevaporated in vacuo
  9. customto afford an oil that
  10. customwas purified by radial chromatography (2 mm plate)
  11. concentrationconcentrated

出典と根拠

ORDレコード
ord-59076620d7f542dbacc2cc7abd315a84
出典データセット
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06649600B1

反応ノート

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