Ethylene Glycol → 13beta-Ethyl-3-methoxy-6-methyl-17,17-ethylenedioxygona-1,3,5(10),8,14-pentaene

HRID 1077225노트

반응식

HRID 1077225 반응식
[CH2:1]([C:3]1([CH2:10][CH2:11][C:12](=O)[CH2:13][CH2:14][CH:15]([C:17]2[CH:22]=[CH:21][CH:20]=[C:19](OC)[CH:18]=2)[CH3:16])[C:7](=O)[CH2:6][CH2:5][C:4]1=O)[CH3:2].[C:26]1(C)C=CC(S(O)(=O)=O)=CC=1.[CH2:37]([OH:40])[CH2:38][OH:39].[OH2:41]>C1C=CC=CC=1>[CH2:1]([C@:3]12[CH2:10][CH2:11][C:12]3[C:18]4[CH:19]=[CH:20][C:21]([O:41][CH3:26])=[CH:22][C:17]=4[CH:15]([CH3:16])[CH2:14][C:13]=3[C:7]1=[CH:6][CH2:5][C:4]12[O:40][CH2:37][CH2:38][O:39]1)[CH3:2]

참가 물질

6

실험 절차

Dissolve 2-ethyl-2-(6-m-methoxyphenyl-6-methyl-3-oxohexyl)-1,3-cyclopentanedione (39.7 g) in benzene (500 ml) and reflux with p-toluenesulfonic acid in water (11.0 g). Remove 2 moles of water, add ethyleneglycol (50 ml) and reflux the solution overnight (16 hours). After working up by the usual procedure, filter repeatedly through Florex in hexane. Recrystallize from ethanol to obtain dl-13β-ethyl-3-methoxy-6-methyl-17,17-ethylenedioxygona-1,3,5(10),8,14-pentaene (16.8 g), m.p. 120°-122°; ultraviolet absorption peak at 312 mμ, no infrared absorption in the ketone region.

후처리

  1. temperaturereflux the solution overnight (16 hours)
  2. filtrationfilter repeatedly through Florex in hexane
  3. customRecrystallize from ethanol

출처 및 근거

ORD 기록
ord-5a65e9efc80147d2a678da880035a74c
출처 데이터셋
uspto-grants-1976_05
특허 번호
US03959322

반응 노트

불러오는 중…