Piperidine → 3-Hydroxy-2-(p-Diethylaminophenyl-methylidene)-1-Indanone

HRID 1679083노트

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HRID 1679083 반응식
[CH2:1]([N:3]([CH2:12][CH3:13])[C:4]1[CH:11]=[CH:10][C:7]([CH:8]=O)=[CH:6][CH:5]=1)[CH3:2].[OH:14][CH:15]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[C:17](=[O:24])[CH2:16]1.N1CCCCC1>ClCCCC>[OH:24][CH:17]1[C:18]2[C:23](=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:15](=[O:14])[C:16]1=[CH:8][C:7]1[CH:10]=[CH:11][C:4]([N:3]([CH2:12][CH3:13])[CH2:1][CH3:2])=[CH:5][CH:6]=1

참가 물질

5

실험 절차

A mixture of 56.6 g.(0.32 mole) of p-diethylaminobenzaldehyde, 47.36 g. (0.32 mole) of 3-hydroxy-1-indanone and 7 ml. of piperidine was then heated with magnetic stirring to 80°-100° C. for 1.5 hours (the mixture is a melt at the reaction temperature). The mixture was cooled in ice water, 90 ml. of 1-chlorobutane and seed was added. The product tended to come out as a gum; the solution was therefore heated, cooled (seeded) and muddy brown solid separated. The product was collected by filtration and the brown solid washed until bright orange; 43.62 g. 44% yield, m.p. 139°-141°, m.p. recrystallized material (1-chlorobutane) 142°-143° C. An extra 11% yield was obtained through concentration and refiltration of the filtrate; the latter fraction washed up as cleanly as the first. The IR spectrum and elemental analysis are those expected of the titled merocyanine derivative.

후처리

  1. additionA mixture of 56.6 g
  2. temperaturethe solution was therefore heated
  3. temperaturecooled (seeded) and muddy brown solid
  4. customseparated
  5. filtrationThe product was collected by filtration
  6. washthe brown solid washed until bright orange
  7. custom44% yield, m.p. 139°-141°, m.p. recrystallized material (1-chlorobutane) 142°-143° C
  8. customAn extra 11% yield was obtained through concentration and refiltration of the filtrate
  9. washthe latter fraction washed up as cleanly as the first

출처 및 근거

ORD 기록
ord-b2cdb93f7f2442ad9bb0f6f4ee8fa1ac
출처 데이터셋
uspto-grants-1978_03
특허 번호
US04078934

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