ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Methoxymethyl-triphenylphosphonium chloride → HCID 178456482、化合物

HRID 480144
ノート
印刷プレビュー

反応式

HRID 480144 の反応式
[Cl-].[CH3:2][O:3]C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C[Si]([N-][Si](C)(C)C)(C)C.[K+].[O:34]=[C:35]1[N:43]([CH2:44][CH2:45][CH3:46])[C:42]2[NH:41][C:40]([C:47]34[CH2:54][CH2:53][C:50]([CH:55]=O)([CH2:51][CH2:52]3)[CH2:49][CH2:48]4)=[N:39][C:38]=2[C:37](=[O:57])[N:36]1[CH2:58][CH2:59][CH3:60]>C1COCC1>[O:34]=[C:35]1[N:43]([CH2:44][CH2:45][CH3:46])[C:42]2[NH:41][C:40]([C:47]34[CH2:54][CH2:53][C:50]([CH2:55][CH:2]=[O:3])([CH2:51][CH2:52]3)[CH2:49][CH2:48]4)=[N:39][C:38]=2[C:37](=[O:57])[N:36]1[CH2:58][CH2:59][CH3:60]
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 2723798Methoxymethyl-triphenylphosphonium chlorideHCID 3251421Potassium bis(trimethylsilyl)amideHCID 178456486HCID 178456486、化合物

生成物 1

HCID 178456482HCID 178456482、化合物収率 75%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a stirred suspension of methoxymethyl triphenylphosphonium chloride (1.1 g, 3.2 mmol) in THF (60 ml) at −78° C. was added a solution of KHMDS (0.5 M in toluene, 10 ml, 5 mmol). The resulting yellow mixture was stirred at this temperature for 1.5 h and 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 (12 ml) was added over a period of 20 minutes. The mixture was held at −78° C. for 6 h and allowed to reach ambient temperature overnight (12 h). The reaction mixture was partitioned between saturated aqeuous NH4Cl (100 ml) and EtOAc (100 ml) and the aqueous phase was extracted with EtOAc (50 ml). The combined organic extracts were washed with saturated aqeuous NaCl (100 ml), concentrated in vacuo, redissolved in THF and concentrated to a volume of approx. 20 ml. To the solution was added an equal volume of 1 N HCl and the mixture was stirred overnight. The mixture was diluted with EtOAc (20 ml), the aqueous phase was separated and extracted with EtOAc (10 ml). The combined organic phases were then washed with saturated aqeuous NaCI (2×, 25 ml), dried (MgSO4), filtered and concentrated in vacuo. The resulting orange oil was purified in batches by radial chromatography (2 mm plate) using 3% MeOH and 3% THF in CH2Cl2 as eluent. Product-containing fractions were combined and concentrated to afford 290 mg (75%) of a white solid. MS: 387 (MH+).

後処理

  1. waitThe mixture was held at −78° C. for 6 h
  2. waitto reach ambient temperature overnight
  3. custom(12 h)
  4. customThe reaction mixture was partitioned between saturated aqeuous NH4Cl (100 ml) and EtOAc (100 ml)
  5. extractionthe aqueous phase was extracted with EtOAc (50 ml)
  6. washThe combined organic extracts were washed with saturated aqeuous NaCl (100 ml)
  7. concentrationconcentrated in vacuo
  8. dissolutionredissolved in THF
  9. concentrationconcentrated to a volume of approx. 20 ml
  10. additionTo the solution was added an equal volume of 1 N HCl
  11. stirringthe mixture was stirred overnight
  12. additionThe mixture was diluted with EtOAc (20 ml)
  13. customthe aqueous phase was separated
  14. extractionextracted with EtOAc (10 ml)
  15. washThe combined organic phases were then washed with saturated aqeuous NaCI (2×, 25 ml)
  16. dry with materialdried (MgSO4)
  17. filtrationfiltered
  18. concentrationconcentrated in vacuo
  19. customThe resulting orange oil was purified in batches by radial chromatography (2 mm plate)
  20. concentrationconcentrated

出典と根拠

ORDレコード
ord-200e77c581e940538eb6138e34ee83b2
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

読み込み中…

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