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Ethylene Oxide → 2,6-Diethyl-1-(2-hydroxyethyl)-2,3,6-trimethyl-4-piperidyl methylcarbamate

HRID 1391242
ノート
印刷プレビュー

反応式

HRID 1391242 の反応式
[CH3:1][NH:2][C:3](=[O:18])[O:4][CH:5]1[CH2:10][C:9]([CH2:12][CH3:13])([CH3:11])[NH:8][C:7]([CH2:15][CH3:16])([CH3:14])[CH:6]1[CH3:17].[CH2:19]1[O:21][CH2:20]1>CO.Cl>[CH3:1][NH:2][C:3](=[O:18])[O:4][CH:5]1[CH2:10][C:9]([CH2:12][CH3:13])([CH3:11])[N:8]([CH2:19][CH2:20][OH:21])[C:7]([CH2:15][CH3:16])([CH3:14])[CH:6]1[CH3:17]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 6354Ethylene OxideHCID 537281202,6-Diethyl-2,3,6-trimethyl-4-piperidyl methylcarbamate

生成物 1

HCID 536336612,6-Diethyl-1-(2-hydroxyethyl)-2,3,6-trimethyl-4-piperidyl methylcarbamate収率 50.2%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid触媒HCID 887Methanol溶媒

反応条件

温度
100 °C

実験手順

To a solution of 5.1 g of 2,6-diethyl-2,3,6-trimethyl-4-piperidyl methylcarbamate (Compound 66 - prepared as described in Preparation 4) in 8 ml of methanol were added 1.74 g of ethylene oxide and 1 drop of concentrated hydrochloric acid. The mixture was heated overnight at 100° C. in a sealed tube. When the reaction was complete, the reaction mixture was concentrated by evaporation under reduced pressure and the residue was purified by column chromatography on silica gel using a 1 : 1 by volume mixture of benzene and ethyl acetate as eluent, giving 3.0 g of Compound 84. The compound showed a single spot on thin layer chromatography on silica gel (developing solvent: benzene/ethyl acetate, 1 : 1 by volume), Rf value 0.51.

後処理

  1. concentrationthe reaction mixture was concentrated by evaporation under reduced pressure
  2. customthe residue was purified by column chromatography on silica gel using a 1 : 1
  3. additionby volume mixture of benzene and ethyl acetate as eluent

出典と根拠

ORDレコード
ord-14ece4b2e9284d4ca5fc6b737cffc251
出典データセット
uspto-grants-1979_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04141883

反応ノート

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