ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Cyclohexylamine → 1H-Pyrrole, 1-cyclohexyl-2,5-dihydro-

HRID 126908
ノート
印刷プレビュー

反応式

HRID 126908 の反応式
[CH:1]1([NH2:7])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Cl[CH:9]=[CH:10][CH2:11][CH2:12]Cl>C1C=CC=CC=1>[CH:1]1([N:7]2[CH2:12][CH:11]=[CH:10][CH2:9]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
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

4

反応物 2

HCID 7965CyclohexylamineHCID 35801CID 35801

生成物 1

HCID 1065901H-Pyrrole, 1-cyclohexyl-2,5-dihydro-収率 76%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

反応条件

温度
92 °C

実験手順

A solution of 5.19 kg (52.3 moles) of cyclohexylamine in 4.0 liters of benzene was heated to mild reflux (92° C.) and then the heating discontinued. To the solution was added, dropwise, 1,635 g (13.1 moles) of 1,4-dichlorobutene at a rate sufficient to maintain gentle reflux, 3 hours time being required. Heat was reapplied and the reactants were heated at reflux temperature for 18 hours. The mixture was cooled to about 50° C. and filtered to remove the hydrochloride. Carbon dioxide was bubbled into the filtrate to precipitate excess amine carbonate which was removed by filtration. Solvent was removed from the filtrate by distillation under reduced pressure and the reddish fluid residue slightly contaminated with benzene weighed 1,506 g (76% yield).

後処理

  1. additionTo the solution was added
  2. temperatureHeat
  3. temperaturethe reactants were heated
  4. temperatureat reflux temperature for 18 hours
  5. temperatureThe mixture was cooled to about 50° C.
  6. filtrationfiltered
  7. customto remove the hydrochloride
  8. customCarbon dioxide was bubbled into the filtrate
  9. customto precipitate excess amine carbonate which
  10. customwas removed by filtration
  11. customSolvent was removed from the filtrate by distillation under reduced pressure

出典と根拠

ORDレコード
ord-b377109ab96d469c846532b1cff41539
出典データセット
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04254135

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート