Dimethyl Sulfoxide → 2-(5-Oxo-3-pentynyl)cyclopropanecarboxylic acid methyl ester

HRID 36812Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 36812
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH3:11][O:12][C:13]([CH:15]1[CH2:17][CH:16]1[CH2:18][CH2:19][C:20]#[C:21][CH2:22][OH:23])=[O:14].C(N(CC)CC)C.[Cl-].[Na+]>ClCCl>[CH3:11][O:12][C:13]([CH:15]1[CH2:17][CH:16]1[CH2:18][CH2:19][C:20]#[C:21][CH:22]=[O:23])=[O:14]

Komponenten

7

Reaktionsbedingungen

Temperatur
-40 °C

Versuchsvorschrift

Oxalyl chloride (0.40 g, 3.1 mmol) was dissolved in dichloromethane, and the solution was cooled to -40° C. A solution of dimethyl sulfoxide (0.52 g, 6.2 mmol) in dichloromethane (2 ml) was added thereto over a period of 5 minutes, and the mixture was stirred for 20 minutes. A solution of 2-(5-hydroxy-3-pentynyl)cyclopropanecarboxylic acid methyl ester (0.37 g, 2 mmol) in dichloromethane (5 ml) was added thereto, and the mixture was stirred for 30 minutes. Then, triethylamine (1.7 ml, 12 mmol) was added thereto. The temperature was raised to 0° C., and a saturated sodium chloride aqueous solution was added thereto. The product was extracted with dichloromethane, dried over anhydrous magnesium sulfate and then purified by silica gel column chromatography to obtain the above identified compound (0.35 g, yield: 96%).

Aufarbeitung

  1. stirringthe mixture was stirred for 30 minutes
  2. temperatureThe temperature was raised to 0° C.
  3. extractionThe product was extracted with dichloromethane
  4. dry with materialdried over anhydrous magnesium sulfate
  5. custompurified by silica gel column chromatography
  6. customto obtain the

Quellen und Nachweise

ORD-Eintrag
ord-4396e180818a44a9afcb702bc14349a3
Quelldatensatz
uspto-grants-1995_05
Patentnummer
US05416231

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