Basic ashless additives and lubricating compositions containing same
A technology of lubricant composition and lubricating viscosity, which is applied in the preparation of lubricating compositions, additives, organic compounds, etc., and can solve problems such as poor durability
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example A
[0143] Example A (comparison)
[0144] Equipped with overhead stirrer, thermocouple, N 2 Ethanol (1000 ml) was added to a 2 L round bottom flask with an inlet and a water-cooled condenser, followed by α-methylbenzylamine (131.3 g), and the mixture was stirred. Ethyl acrylate (108.5 g) was added thereto over a period of 4 hours. The reaction was allowed to exotherm. The reaction mixture was then stirred for an additional 3 hours and then left to stand overnight. The reaction mixture was then concentrated under reduced pressure to remove ethanol. The resulting liquid was then vacuum stripped at 110° C. at a pressure of 0 to 20 mbar. This yielded 226.6 g of ethyl 3-((1-phenylethyl)amino)propanoate.
example B
[0145] Example B (comparison)
[0146] Equipped with overhead stirrer, thermocouple, N 2 Acetonitrile (1500ml), α-methylbenzylamine (100g), potassium carbonate (250.9g), and potassium iodide (24.7g) were added to the inlet and 3L jacketed vessel of the water-cooled condenser. To the stirred mixture was added ethyl chloroacetate (197.1 g) over a period of 1 hour and the reaction was stirred at room temperature for 2 hours. The reaction was heated to 50°C for 5 hours, then heated to 70°C and stirred for 7 hours. The reaction mixture was cooled to room temperature and filtered. The filtrate was concentrated under reduced pressure and filtered again. This yielded 188 g of diethyl 2,2'-((1-phenylethyl)azadiyl)diacetate.
example C
[0148] N-Benzylglycine ethyl ester was purchased commercially from Sigma-Aldrich, Inc.
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