Sodium hydride → HCID 20287596, Verbindung

HRID 127089

Reaktionsgleichung

Reaktionsgleichung von HRID 127089
[H-].[Na+].[C:3]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[C:13](=[O:17])[CH2:14][CH2:15][CH:16]=1)(O)=[O:4].C(Cl)(=O)C([Cl:21])=O>O1CCCC1.CCOCC>[Cl:21][C:3]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[C:13](=[O:17])[CH2:14][CH2:15][CH:16]=1)=[O:4]

Komponenten

6

Edukt 3

HCID 24758Sodium hydrideHCID 65578Oxalyl chlorideHCID 789025-Oxo-1-cyclopentene-1-heptanoic acid

Produkt 1

HCID 20287596HCID 20287596, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3283Diethyl EtherLösungsmittelHCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a suspension of 1.94 g (0.08 mol) of sodium hydride in 100 ml of tetrahydrofuran is added with stirring under argon dropwise a solution of 17 g (0.08 mol) of 2-(6-carboxyhexyl)cyclopent-2-en-1-one in 160 ml of tetrahydrofuran. After the addition is complete, the mixture is stirred for 1 hour 15 minutes. The mixture is cooled to 0° C. and 13 ml of oxalyl chloride is added. The mixture is stirred at 0° C. for 30 minutes and at room temperature for 30 minutes. The solution is diluted with 500 ml of ether and filtered through Celite. The solvent is removed from the filtrate and the residue is extracted with hot hexane twice. The hexane is removed to give 16.0 g of the title compound.

Aufarbeitung

  1. additionis added
  2. additionAfter the addition
  3. stirringThe mixture is stirred at 0° C. for 30 minutes and at room temperature for 30 minutes
  4. filtrationfiltered through Celite
  5. customThe solvent is removed from the filtrate
  6. extractionthe residue is extracted with hot hexane twice
  7. customThe hexane is removed

Quellen und Nachweise

ORD-Eintrag
ord-1ae4d7594c9d4be0af8f2fd7dc9e0ea2
Quelldatensatz
uspto-grants-1981_03
Patentnummer
US04254285

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