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Ethyl 4-oxocyclohexanecarboxylate → HCID 18340695、化合物

HRID 714511
ノート
印刷プレビュー

反応式

HRID 714511 の反応式
[Cl-].[Li+].C(OP([CH2:11][C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])(OCC)=O)C.O=[C:20]1[CH2:25][CH2:24][CH:23]([C:26]([O:28][CH2:29][CH3:30])=[O:27])[CH2:22][CH2:21]1>CC#N>[C:15]([O:14][C:12](=[O:13])[CH:11]=[C:20]1[CH2:25][CH2:24][CH:23]([C:26]([O:28][CH2:29][CH3:30])=[O:27])[CH2:22][CH2:21]1)([CH3:16])([CH3:17])[CH3:18]
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 317638Ethyl 4-oxocyclohexanecarboxylateHCID 433294Lithium ChlorideHCID 2773685tert-Butyl diethylphosphonoacetate

生成物 1

HCID 18340695HCID 18340695、化合物収率 62.1%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

To a suspension of anhydrous lithium chloride (1.9 g, 45 mmol) in MeCN (100 ml) was added tert-butyl 2-(diethoxyphosphoryl)acetate (7.6 g, 30 mmol) at room temperature. The mixture was stirred for 30 min. TEA (6.4 ml, 45 mmol) was added and the mixture was stirred for another 30 min. Ethyl 4-oxocyclohexanecarboxylate (5.1 g, 30 mmol) was added and the mixture was stirred overnight. The precipitate was filtered off and the filtrate was concentrated to afford brown oil, which was purified by silica gel column (PE:EtOAc=10:1) to afford product (5 g, 62%).

後処理

  1. stirringthe mixture was stirred for another 30 min
  2. stirringthe mixture was stirred overnight
  3. filtrationThe precipitate was filtered off
  4. concentrationthe filtrate was concentrated
  5. customto afford brown oil, which
  6. customwas purified by silica gel column (PE:EtOAc=10:1)

出典と根拠

ORDレコード
ord-d6bc09e0770f4cd694958a3123fba500
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09187447B2

反応ノート

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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