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HRID 1250432Erstellt: 25. Oktober 2026

Triethylamine → 2-Acetoxy-N-ethyl-N-(3,3,5-trimethyl-cyclohexa-1,5-dienyl)-acetamide

https://huagongshe.com/reaction/1250432

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktAcetoxyacetyl chlorideHCID 26297—
EduktEthyl-(3,5,5-trimethyl-cyclohex-2-enylidene)-amineHCID 11205971—
LösungsmittelTolueneHCID 1140—
Produkt2-Acetoxy-N-ethyl-N-(3,3,5-trimethyl-cyclohexa-1,5-dienyl)-acetamideHCID 112885591.076,8%

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

2-Acetoxyacetyl chloride (6.42 g, 4.7 mmol) is added slowly to a mixture of 1A (7.62 g, 4.2 mmol) and toluene (50 ml), which is cooled to −5° C. After the addition is complete, the mixture is stirred for a further 1 hour at −5° C., then allowed to warm to room temperature and stirred for a further 1.5 hours. The reaction mixture is then cooled down to −3° C. and a mixture of triethylamine (6.5 ml, 4.7 mmol) and toluene (25 ml) is added slowly to the mixture. The mixture is stirred for a further 16 hours, during which time the temperature is gradually allowed to rise to room temperature. The mixture is filtered, and the filtrate is washed three times with water, dried over sodium sulfate and evaporated in vacuo to give the crude product (12.0 g, 89%) as an oil. A portion of this crude material (4 g) is purified by flash column chromatography, eluting with a mixture of ethyl acetate and petroleum ether (1:4) to give pure product (2.3 g, equivalent to 51% overall), with m.p. 38-40° C. NMR analysis of this indicates that the product has a purity of about 88 mol %, the impurity consisting mainly of two isomeric products.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06339042B1
Quelldatensatzuspto-grants-2002_01
ORD IDord-5eb2251a85054bc2a025b6ef0e74e733
Quellennotizuspto-grants-2002_01