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Hydrochloric Acid → 7-[2,3-Dihydroxy-5-(3-hydroxyoct-1-enyl)cyclopentyl]heptanoic acid

HRID 372136
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 372136
[OH:1][CH:2]1[CH:6]([O:7]C2CCCCO2)[CH2:5][CH:4]([CH:14]=[CH:15][CH:16]([OH:22])[CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])[CH:3]1[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][C:29]([OH:31])=[O:30].Cl>C(O)C>[OH:1][CH:2]1[CH:6]([OH:7])[CH2:5][CH:4]([CH:14]=[CH:15][CH:16]([OH:22])[CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])[CH:3]1[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][C:29]([OH:31])=[O:30]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 313Hydrochloric AcidHCID 543618807-[2-Hydroxy-5-(3-hydroxyoct-1-enyl)-3-(2-tetrahydropyranyloxy)cyclopentyl]heptanoic acid

Produkt 1

HCID 542209287-[2,3-Dihydroxy-5-(3-hydroxyoct-1-enyl)cyclopentyl]heptanoic acidAusbeute 3,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

A mixture of 7-[2-hydroxy-5-(3-hydroxyoct-1enyl)-3-(2-tetrahydropyranyloxy)cyclopentyl]heptanoic acid [0.34 g.; prepared as described above in Example 2(h)], ethanol (10 ml.), N aqueous hydrochloric acid (10 ml.) and a cation exchange resin [Dowex resin AG50W-X 8H+ (1.0 g.)] was stirred at 60°-62° C. for 8 hours. The mixture was filtered and the solid was washed with ethanol. The combined filtrate and washings were concentrated in vacuo to remove most of the ethanol, and the residue was extracted twice with diethyl ether. The combined ethereal extracts were extracted with 2N aqueous sodium carbonate solution, and the aqueous extract was acidified to pH 1 by the addition of concentrated hydrochloric acid. The resulting aqueous mixture was extracted with diethyl ether and the ethereal extract was dried over magnesium sulphate and evaporated to dryness. The residue (0.13 g.) was subjected to preparative thin-layer chromatography on silica gel, using a mixture of ethyl acetate, cyclohexane and formic acid (40:40:1 by volume) as the eluent, to give 7-[2,3-dihydroxy-5-(3-hydroxyoct-1-enyl)cyclopentyl]heptanoic acid (0.01 g.), νmax 1700 cm-1, 980 cm-1. Elemental analysis: found: C, 67.8; H, 10.4%; C20H36O5 requires C, 67.4; H, 10.2%.

Aufarbeitung

  1. filtrationThe mixture was filtered
  2. washthe solid was washed with ethanol
  3. concentrationThe combined filtrate and washings were concentrated in vacuo
  4. customto remove most of the ethanol
  5. extractionthe residue was extracted twice with diethyl ether
  6. extractionThe combined ethereal extracts were extracted with 2N aqueous sodium carbonate solution
  7. extractionthe aqueous extract
  8. additionwas acidified to pH 1 by the addition of concentrated hydrochloric acid
  9. extractionThe resulting aqueous mixture was extracted with diethyl ether
  10. extractionthe ethereal extract
  11. dry with materialwas dried over magnesium sulphate
  12. customevaporated to dryness
  13. additiona mixture of ethyl acetate, cyclohexane and formic acid (40:40:1 by volume) as the eluent

Quellen und Nachweise

ORD-Eintrag
ord-7b4cff3be016492880d8a0848e561946
Quelldatensatz
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04088821

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