Carbon Dioxide → 7-(4-Methoxyphenyl)heptyl phenyl sulfide

HRID 839162노트

반응식

HRID 839162 반응식
C1([Li])C=CC=CC=1.[C:8]1([S:14][CH3:15])[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.C(=O)=O.[CH3:19][O:20][C:21]1[CH:26]=[CH:25][C:24]([CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32]I)=[CH:23][CH:22]=1>O.O1CCCC1>[C:8]1([S:14][CH2:15][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][C:24]2[CH:23]=[CH:22][C:21]([O:20][CH3:19])=[CH:26][CH:25]=2)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

참가 물질

7

실험 절차

Phenyllithium (378 ml., 0.755 mole) was added over a period of 2-5 minutes to a solution of 94.5 g. of thioanisole in 600 ml. of tetrahydrofuran, stirred under nitrogen. The mixture was stirred at room temperature for about 16 hours, then cooled to -70° C. (solid CO2), and 141 g. of 6-(4-methoxyphenyl)hexyl iodide in 210 ml. of tetrahydrofuran was added slowly. The reaction mixture was stirred at -65° C. for 2 hours and then allowed to warm to room temperature. Water was added and the mixture extracted with pentane. The pentane extracts were washed with water, dried and concentrated to remove the solvent. The residue was distilled in vacuo, b.p. 171°-174° C. (0.15 mm.). The distillate crystallized and was recrystallized from pentane, to give 7-(4-methoxyphenyl)heptyl phenyl sulfide, m.p. 58°-59° C.

후처리

  1. stirringThe reaction mixture was stirred at -65° C. for 2 hours
  2. temperatureto warm to room temperature
  3. extractionthe mixture extracted with pentane
  4. washThe pentane extracts were washed with water
  5. customdried
  6. concentrationconcentrated
  7. customto remove the solvent
  8. distillationThe residue was distilled in vacuo, b.p. 171°-174° C. (0.15 mm.)
  9. customThe distillate crystallized
  10. customwas recrystallized from pentane

출처 및 근거

ORD 기록
ord-a638036b5dba45769a6e9b7d5f0c2bf3
출처 데이터셋
uspto-grants-1978_06
특허 번호
US04093736

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