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Potassium Carbonate → (R)-2,2-difluoro-hexahydro-5,5-dimethylindolizin-7(1H)-one

HRID 633349
ノート
印刷プレビュー

反応式

HRID 633349 の反応式
[F:1][C:2]1([F:14])[CH2:6][NH:5][C@H:4]([CH2:7][C:8](=[O:13])[CH:9]=[C:10]([CH3:12])[CH3:11])[CH2:3]1.C([O-])([O-])=O.[K+].[K+]>CO>[F:14][C:2]1([F:1])[CH2:6][N:5]2[C@H:4]([CH2:7][C:8](=[O:13])[CH2:9][C:10]2([CH3:11])[CH3:12])[CH2:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 11430Potassium CarbonateHCID 867044601-((R)-4,4-difluoropyrrolidin-2-yl)-4-methylpent-3-en-2-one

生成物 1

HCID 86704459(R)-2,2-difluoro-hexahydro-5,5-dimethylindolizin-7(1H)-one収率 69%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A MeOH (350 ml) solution of 1-((R)-4,4-difluoropyrrolidin-2-yl)-4-methylpent-3-en-2-one and K2CO3 (2.5 g, 18 mmol) was stirred at 40° C. for 15 hours, the reaction went to completion as monitored by LC-MS. Solvent was removed in vacuo, remaining material was suspended in CH2Cl2, solid was filtered off, filtrate was collected and solvent was removed in vacuo. Product was purified by silica gel chromatography (Hexane/EtOAc, linear gradient from 100:0 to 80:20). Compound (R)-2,2-difluoro-hexahydro-5,5-dimethylindolizin-7(1H)-one was obtained as a light yellow solid: 637.4 mg (69% yield over 3 steps).

後処理

  1. customSolvent was removed in vacuo
  2. filtrationsolid was filtered off
  3. customfiltrate was collected
  4. customsolvent was removed in vacuo
  5. customProduct was purified by silica gel chromatography (Hexane/EtOAc, linear gradient from 100:0 to 80:20)

出典と根拠

ORDレコード
ord-c7a2665a97194efba2650730c0d0d64b
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09321763B2

反応ノート

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