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Morpholine → 3-Methyl-1-morpholinobutadiene

HRID 486839
ノート
印刷プレビュー

反応式

HRID 486839 の反応式
C(=O)([O-])[O-].[K+].[K+].[NH:7]1[CH2:12][CH2:11][O:10][CH2:9][CH2:8]1.[CH3:13][C:14]([CH3:18])=[CH:15][CH:16]=O>C1(C)C=CC=CC=1>[CH3:18][C:14](=[CH2:13])[CH:15]=[CH:16][N:7]1[CH2:12][CH2:11][O:10][CH2:9][CH2:8]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

5

反応物 3

HCID 8083MorpholineHCID 11430Potassium CarbonateHCID 610203-Methyl-2-butenal

生成物 1

HCID 5867713-Methyl-1-morpholinobutadiene

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
0 °C

実験手順

Anhydrous potassium carbonate (43.5 mmol; 6 g) and morpholine (308 mmol; 26.8 g) were introduced into a 100-ml Erlenmeyer equipped with a dropping funnel, under an inert atmosphere. When the reaction medium had been cooled to 0° C., prenal (150 mmol) in toluene (20 ml) was added dropwise. The temperature was allowed to rise to 20° C. and stirring was continued for 4 hours. The potassium carbonate was separated by filtration. The toluene was removed at atmospheric pressure, which permits cracking of the aminal. Under reduced pressure, the excess morpholine was distilled first, and then the expected dienamine (b.p. 108°-110° C. at 20 mm Hg) was distilled.

後処理

  1. customequipped with a dropping funnel, under an inert atmosphere
  2. customto rise to 20° C.
  3. customThe potassium carbonate was separated by filtration
  4. customThe toluene was removed at atmospheric pressure, which
  5. distillationUnder reduced pressure, the excess morpholine was distilled first
  6. distillationthe expected dienamine (b.p. 108°-110° C. at 20 mm Hg) was distilled

出典と根拠

ORDレコード
ord-cab6972fc8884bc09b38c60c34d1b733
出典データセット
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05292897

反応ノート

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