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

HRID 1413824
ノート
印刷プレビュー

反応式

HRID 1413824 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-

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. Heating was continued 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 salt. Carbon dioxide was bubbled into the filtrate to precipitate excess amine carbonate salt 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 (76.2 yield).

後処理

  1. additionTo the solution was added
  2. temperatureHeating
  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 salt
  8. customCarbon dioxide was bubbled into the filtrate
  9. customto precipitate excess amine carbonate salt which
  10. customwas removed by filtration
  11. customSolvent was removed from the filtrate by distillation under reduced pressure
  12. custom1.506 g (76.2 yield)

出典と根拠

ORDレコード
ord-ba0f7a92ac4b41b891e04d0e569dfd11
出典データセット
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04251541

反応ノート

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