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Water → 2-Ethyl-2,5-dimethyl-1-azaspiro[5.5]undecan-4-one

HRID 616538
ノート
印刷プレビュー

反応式

HRID 616538 の反応式
[CH2:1]([C:3]1[CH2:8][C:7]([CH2:10][CH3:11])([CH3:9])[NH:6][C:5]2([CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)N=1)[CH3:2].[Br-].[NH4+].[OH2:19]>CO>[CH2:10]([C:7]1([CH3:9])[CH2:8][C:3](=[O:19])[CH:1]([CH3:2])[C:5]2([CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)[NH:6]1)[CH3:11]
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 962WaterHCID 25514Ammonium BromideHCID 213304542,4-Diethyl-4-methyl-1,5-diazaspiro[5.5]undec-1-ene

生成物 1

HCID 213304692-Ethyl-2,5-dimethyl-1-azaspiro[5.5]undecan-4-one

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

11.1 g of the 2,4-diethyl-4-methyl-1,5-diazaspiro[5.5]-undec-1-ene thus obtained and 2.5 g of ammonium bromide were dissolved in 70 ml of methanol. 45 ml of water were added to the solution, with stirring. The mixture was then stirred at room temperature for 8 hours. Methanol was removed by evaporation under reduced pressure and the residue was then distilled under reduced pressure, giving 7.4 g of the title product, bp 119° - 122° C/1.5 mmHg.

後処理

  1. stirringThe mixture was then stirred at room temperature for 8 hours
  2. customMethanol was removed by evaporation under reduced pressure
  3. distillationthe residue was then distilled under reduced pressure

出典と根拠

ORDレコード
ord-7b2bd52ea2a143af9a89c30e34c19a40
出典データセット
uspto-grants-1978_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04075165

反応ノート

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