Sodium Hydroxide → [[8-Acetyl-7-[3-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)propoxy]propoxy]-2-naphthalenyl]oxy]acetic acid

HRID 1719411노트

반응식

HRID 1719411 반응식
C[O:2][C:3](=[O:41])[CH2:4][O:5][C:6]1[CH:15]=[CH:14][C:13]2[C:8](=[C:9]([C:38](=[O:40])[CH3:39])[C:10]([O:16][CH2:17][CH2:18][CH2:19][O:20][CH2:21][CH2:22][CH2:23][O:24][C:25]3[CH:30]=[CH:29][C:28]([C:31](=[O:33])[CH3:32])=[C:27]([OH:34])[C:26]=3[CH2:35][CH2:36][CH3:37])=[CH:11][CH:12]=2)[CH:7]=1.[OH-].[Na+]>CO>[C:38]([C:9]1[C:10]([O:16][CH2:17][CH2:18][CH2:19][O:20][CH2:21][CH2:22][CH2:23][O:24][C:25]2[CH:30]=[CH:29][C:28]([C:31](=[O:33])[CH3:32])=[C:27]([OH:34])[C:26]=2[CH2:35][CH2:36][CH3:37])=[CH:11][CH:12]=[C:13]2[C:8]=1[CH:7]=[C:6]([O:5][CH2:4][C:3]([OH:41])=[O:2])[CH:15]=[CH:14]2)(=[O:40])[CH3:39]

참가 물질

4

실험 절차

A mixture of 1.2 g of [[8-acetyl-7-[3-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)propoxy]propoxy]-2-naphthalenyl]oxy]acetic acid methyl ester and 21 ml of 1N sodium hydroxide in 42 ml of methanol was stirred at reflux for 1 hour. The methanol was removed in vacuo and the aqueous solution was washed with ethyl acetate. The aqueous layer was acidified with 3N hydrochloric acid to pH 3 and the oil was extracted with chloroform. The extract was dried (magnesium sulfate) and concentrated to give an oil which was triturated with ether-cyclohexane and filtered to yield 0.85 g, mp 101°-104° C. (73%) of [[8-acetyl-7-[3-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)propoxy]propoxy]-2-naphthalenyl]oxy]acetic acid.

후처리

  1. temperatureat reflux for 1 hour
  2. customThe methanol was removed in vacuo
  3. washthe aqueous solution was washed with ethyl acetate
  4. extractionthe oil was extracted with chloroform
  5. dry with materialThe extract was dried (magnesium sulfate)
  6. concentrationconcentrated
  7. customto give an oil which
  8. customwas triturated with ether-cyclohexane
  9. filtrationfiltered

출처 및 근거

ORD 기록
ord-03b092c7d704463caf717206ea6d900a
출처 데이터셋
uspto-grants-1985_09
특허 번호
US04539419

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