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Water → 5-Cyclododecylidenepentanoic acid

HRID 27303
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 27303
[Na].[Br-].[C:3]([CH2:6][CH2:7][CH2:8][CH2:9][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([OH:5])=[O:4].[C:29]1(=O)[CH2:40][CH2:39][CH2:38][CH2:37][CH2:36][CH2:35][CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1.O>CS(C)=O>[C:29]1(=[CH:9][CH2:8][CH2:7][CH2:6][C:3]([OH:5])=[O:4])[CH2:40][CH2:39][CH2:38][CH2:37][CH2:36][CH2:35][CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 962WaterHCID 13246CyclododecanoneHCID 161236(4-Carboxybutyl)triphenylphosphonium bromideHCID 5360545Sodium

Produkt 1

HCID 233444885-Cyclododecylidenepentanoic acidAusbeute 37,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 679
Dimethyl Sulfoxide
Lösungsmittel
3×

Versuchsvorschrift

Dry dimethylsulfoxide (50 ml, distilled from calcium hydride) and 24.1 ml (0.06 mole) of the sodium salt of dimethylsulfoxide (2.49 M in dimethylsulfoxide, Fieser and Fieser, "Reagents for Organic Synthesis", 1:310 [1967]) were mixed together and cooled in an ice-water bath. Then 13.29 g (0.03 mole) of (4-carboxybutyl) triphenylphosphonium bromide (Aldrich Chemical Co.) was added thereto and the mixture was stirred for 30 min. Cyclododecanone (3.64 g, 0.02 mole; Aldrich Chemical Co.: Beilstein 7[2],36) was dissolved in 10 ml of dry dimethylsulfoxide and added to the above mixture and the mixture was stirred for 15 hr at room temperature. The resulting mixture was then poured into 500 ml of water. This aqueous mixture was extracted with 900 ml (3×300 ml) of ether-ethyl acetate (1:1 V/V). The aqueous phase was acidified (pH 1 to 2) with 30 ml of concentrated hydrochloric acid. The aqueous phase was then extracted with 900 ml (3×300 ml) of ether-hexane (1:1 V/V). The ether-hexane extract was then dried over anhydrous magnesium sulfate, filtered, and the solvent removed in vacuo. The resultant product was recrystallized from ethanol-water to yield 2.0 g (36.2%) of 5-cyclododecylidenepentanoic acid (mp 70°-72° C.) having the following physical characteristics:

Aufarbeitung

  1. temperaturecooled in an ice-water bath
  2. additionadded to the above mixture
  3. stirringthe mixture was stirred for 15 hr at room temperature
  4. extractionThis aqueous mixture was extracted with 900 ml (3×300 ml) of ether-ethyl acetate (1:1 V/V)
  5. extractionThe aqueous phase was then extracted with 900 ml (3×300 ml) of ether-hexane (1:1 V/V)
  6. extractionThe ether-hexane extract
  7. dry with materialwas then dried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. customthe solvent removed in vacuo
  10. customThe resultant product was recrystallized from ethanol-water

Quellen und Nachweise

ORD-Eintrag
ord-e931e1457e44498fb22b657cca35947f
Quelldatensatz
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04220795

Notizen zur Reaktion

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