Triethylamine → HCID 58997533, compound

Participants

Reaction Conditions

Reaction Steps

To a solution of 28 g (0.17 mole) of 2-butyl-2-ethyl-1,3-propandiol in 300 mL of toluene is added dropwise 16 mL (0.17 mole) of phosphorus trichloride at 70° C. After 1 h, the P31-NMR shows that the PCl3 (signal at 220 ppm) is fully reacted and a new product is formed (signal at 150 ppm). The temperature is raised to 80° C. At this temperature a solution of 35.8 g (0.17 mole) 4-nonylcyclohexanol, 200 mL (1.4 mole) of triethylamine in 200 mL of toluene is added rapidly dropwise (approx. 30 min). A suspension is obtained. The P31-NMR—after further 2 h of reaction time—shows that the educt (signal at 150 ppm) is fully reacted and a new product is formed (signal at 123 ppm). After filtration and removal of the toluene (rotary evaporator) the product is isolated. Yield: 68 g (0.165 mol=96% of theory) of the title compound as a crude slight yellow oil; P31-NMR signals at: 124 ppm (major peak); 123 ppm; Total reaction time: 3 h. % P(calc): 7.47; % P (found): 7.24.

Provenance & Evidence