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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Morpholine → 3-Methyl-1-morpholinobutadiene

HRID 486839
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HRID 486839 반응식
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
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참가 물질

5

반응물 3

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

생성물 1

HCID 5867713-Methyl-1-morpholinobutadiene

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
0 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-cab6972fc8884bc09b38c60c34d1b733
출처 데이터셋
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05292897

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