Potassium Carbonate → 1-Benzyl 4-ethyl 5-oxoazepane-1,4-dicarboxylate

HRID 528721ノート

反応式

HRID 528721 の反応式
[CH2:1]([O:8][C:9]([N:11]1[CH2:16][CH2:15][C:14](=[O:17])[CH2:13][CH2:12]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N+](=[CH:20][C:21]([O:23][CH2:24][CH3:25])=[O:22])=[N-].C(=O)([O-])[O-].[K+].[K+]>CCOCC>[CH2:24]([O:23][C:21]([CH:20]1[C:14](=[O:17])[CH2:13][CH2:12][N:11]([C:9]([O:8][CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)=[O:10])[CH2:16][CH2:15]1)=[O:22])[CH3:25]

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 12192Ethyl diazoacetateHCID 643496Benzyl 4-oxopiperidine-1-carboxylate

生成物 1

HCID 146001211-Benzyl 4-ethyl 5-oxoazepane-1,4-dicarboxylate

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒3 回

実験手順

To 1.0 g (4.28 mmol) 4-oxo-piperidine-1-carboxylic acid benzyl ester in 5 mL anhydrous ether maintained between −25° C. and −30° C. were added, over 20 minutes, solutions of 0.7 mL (5.56 mmol) BF3Et2O in 1.5 mL anhydrous ether, followed by 0.67 mL (6.42 mmol) ethyl diazoacetate in 1.5 mL anhydrous ether, and the reaction was maintained between −25° C. and −30° C. for 1 hour. The mixture was allowed to warm up to room temperature, 10 mL 30% potassium carbonate solution was added and the mixture extracted with EtOAc (3×15 mL), the organic layers were combined and dried with MgSO4. After filtration and evaporation of the solvent the product was purified by flash column chromatography (silica, hexane/EtOAc 9:1 to 8:2).

後処理

  1. additionwere added, over 20 minutes
  2. temperaturethe reaction was maintained between −25° C. and −30° C. for 1 hour
  3. extractionthe mixture extracted with EtOAc (3×15 mL)
  4. dry with materialdried with MgSO4
  5. filtrationAfter filtration and evaporation of the solvent the product
  6. customwas purified by flash column chromatography (silica, hexane/EtOAc 9:1 to 8:2)

出典と根拠

ORDレコード
ord-8e0534d993764191aeea71fac17d9e6f
出典データセット
uspto-grants-2016_05
特許番号
US09346816B2

反応ノート

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