Sodium Hydroxide → 7-[3,4-Dihydroxy-2-(3-hydroxyoctyl)cyclopentyl]heptanoic acid

HRID 1580788Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1580788
[OH:1][CH:2]1[CH:6]([OH:7])[CH2:5][CH:4]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([O:16]CC)=[O:15])[CH:3]1[CH2:19][CH2:20][CH:21]([OH:27])[CH2:22][CH2:23][CH2:24][CH2:25][CH3:26].[OH-].[Na+]>C(O)C>[OH:1][CH:2]1[CH:6]([OH:7])[CH2:5][CH:4]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([OH:16])=[O:15])[CH:3]1[CH2:19][CH2:20][CH:21]([OH:27])[CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]

Komponenten

4

Versuchsvorschrift

Ethyl 7-[3,4-dihydroxy-2-(3-hydroxyoctyl)cyclopentyl]heptanoate (2.6 g.) [prepared as described in (p) above], ethanol (50 ml.) and 2N aqueous sodium hydroxide solution (50 ml.) were heated together at reflux for 18 hours. The ethanol was removed in vacuo, water (25 ml.) was added and the mixture was washed with diethyl ether. The aqueous phase { which has a solution of sodium 7-[3,4-dihydroxy-2-(3-hydroxyoctyl)cyclopentyl]heptanoate} was acidified to pH 1 by the dropwise addition of concentrated hydrochloric acid, extracted with diethyl ether, and the ethereal extract dried over magnesium sulphate and evaporated in vacuo to give 7-[3,4-dihydroxy-2-(3-hydroxyoctyl)cyclopentyl]heptanoic acid (1.1 g.).

Aufarbeitung

  1. temperatureat reflux for 18 hours
  2. customThe ethanol was removed in vacuo, water (25 ml.)
  3. additionwas added
  4. washthe mixture was washed with diethyl ether
  5. additionwas acidified to pH 1 by the dropwise addition of concentrated hydrochloric acid
  6. extractionextracted with diethyl ether
  7. extractionthe ethereal extract
  8. dry with materialdried over magnesium sulphate
  9. customevaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-5bdcefae24d04e6a8d46ce443f55993e
Quelldatensatz
uspto-grants-1976_01
Patentnummer
US03933890

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