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Benzylamine → N-[2-(Cyclopentyl)ethyl]benzenemethanamine

HRID 1164941
ノート
印刷プレビュー

反応式

HRID 1164941 の反応式
[C:1]1([CH2:7][NH2:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Br[CH2:10][CH2:11][CH:12]1[CH2:16][CH2:15][CH2:14][CH2:13]1>C(#N)C>[CH:12]1([CH2:11][CH2:10][NH:8][CH2:7][C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[CH2:16][CH2:15][CH2:14][CH2:13]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 7504BenzylamineHCID 12711948(2-Bromoethyl)cyclopentane

生成物 1

HCID 19863445N-[2-(Cyclopentyl)ethyl]benzenemethanamine

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

Combine 10.7 g (0.1 mol) of benzenemethanamine and 17.7 g (0.1 mol) of (2-bromoethyl)cyclopentane in 100 mL of acetonitrile. Heat the mixture to reflux and follow the progress of the reaction by thin-layer chromatography on silica gel. At the completion of the reaction remove the solvent in vacuo and add 100 mL of saturated sodium bicarbonate solution. Extract the aqueous mixture with three 100 mL portions of diethyl ether. Dry the combined extracts over anhydrous sodium sulfate. Filter the drying agent and remove the solvent in vacuo to obtain the title compound.

後処理

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
  1. temperatureHeat the mixture
  2. temperatureto reflux
  3. customthe progress of the reaction by thin-layer chromatography on silica gel
  4. customAt the completion of the reaction remove the solvent in vacuo
  5. additionadd 100 mL of saturated sodium bicarbonate solution
  6. extractionExtract the aqueous mixture with three 100 mL portions of diethyl ether
  7. dry with materialDry the combined extracts over anhydrous sodium sulfate
  8. filtrationFilter the drying agent
  9. customremove the solvent in vacuo

出典と根拠

ORDレコード
ord-295ee8f833594ea1ae7a276a0e44e933
出典データセット
uspto-grants-1990_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04906634

反応ノート

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