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Triethyl phosphonoacetate → tert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-[(1E)-3-ethoxy-3-oxoprop-1-en-1-yl]-1,4-oxazepane-4-carboxylate

HRID 1022672
ノート
印刷プレビュー

反応式

HRID 1022672 の反応式
[Cl-].[Li+].C1(C2CCCCCCCCCC=2)CCCCCCCCNN=1.[CH2:25]([O:27][C:28](=[O:38])[CH2:29]P(OCC)(OCC)=O)[CH3:26].[Cl:39][C:40]1[CH:41]=[C:42]([C@@H:47]2[O:53][CH2:52][CH2:51][N:50]([C:54]([O:56][C:57]([CH3:60])([CH3:59])[CH3:58])=[O:55])[CH2:49][C@H:48]2[CH:61]=O)[CH:43]=[CH:44][C:45]=1[Cl:46]>C(#N)C>[Cl:39][C:40]1[CH:41]=[C:42]([C@@H:47]2[O:53][CH2:52][CH2:51][N:50]([C:54]([O:56][C:57]([CH3:60])([CH3:59])[CH3:58])=[O:55])[CH2:49][C@H:48]2/[CH:61]=[CH:29]/[C:28]([O:27][CH2:25][CH3:26])=[O:38])[CH:43]=[CH:44][C:45]=1[Cl:46]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 13345Triethyl phosphonoacetateHCID 433294Lithium ChlorideHCID 536302743-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 86663853tert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-formyl-1,4-oxazepane-4-carboxylate

生成物 1

HCID 66976531tert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-[(1E)-3-ethoxy-3-oxoprop-1-en-1-yl]-1,4-oxazepane-4-carboxylate

試薬・触媒・溶媒

1
HCID 6342Acetonitrile溶媒

実験手順

To a solution of lithium chloride (136 mg) and diazabicycloundecene (0.403 mL) in acetonitrile (26.7 mL) was added ethyl(diethoxyphosphoryl)acetate (0.642 mL), and the mixture was stirred at 20 min. tert-Butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-formyl-1,4-oxazepane-4-carboxylate (1.00 g) was added and the mixture was stirred overnight. The reaction mixture was concentrated under reduced pressure, distilled water was added, and the mixture was extracted with ethyl acetate. The extract was washed with distilled water and brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (hexane/ethyl acetate) to give the title compound (902 mg).

後処理

  1. additionwas added
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. distillationdistilled water
  4. additionwas added
  5. extractionthe mixture was extracted with ethyl acetate
  6. washThe extract was washed with distilled water and brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. customthe solvent was evaporated under reduced pressure
  9. customThe residue was purified by silica gel chromatography (hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-1cadf7c38a29422cac3f4ee99ee9b35c
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08722662B2

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