Nitrogen → HCID 69309381, compound

Participants

Reaction Steps

To a 250 mL flame dried RBF, LAH (1.43 g, 38.7 mmol) and a magnetic stir bar were added. The flask was sealed with a rubber septum into which N2 inlet/outlet needles were added. Dry ether (10 mL) was added via a syringe to the RBF to wet the LAH. Some gas was evolved. Methyl-3,5-diundecoxybenzoate (15.0 g, 31.5 mmol) was dissolved in dry ether (120 mL) and then cautiously added to the flask via a syringe over a period of 20 minutes. The dark grey solution was left to stir overnight. After approximately 18 hours, water (12 mL) was added very cautiously (drop wise) until the solution color changed to bright white. The contents of the RBF were then transferred to a 2 L separatory funnel. The RBF was alternately rinsed 3 times with distilled H2O (20 mL) and ether (20 mL). One final rinse was made with 1M HCl (20 mL). All rinses were emptied into the separatory funnel. Distilled H2O (200 mL) and ether (200 mL) were added to the separatory funnel. The contents of the separatory funnel were separated into an aqueous layer and an ether layer. The aqueous layer was washed 3 times with ether (200 mL). Ether washes were added to the ether layer. The ether layer was then washed 3 times with distilled H2O (200 mL), once with saturated NaCl (125 mL) and then dried with MgSO4. MgSO4 was removed using gravity filtration. The ether layer was then concentrated using rotary evaporation. The result was a colorless viscous liquid. The liquid solidified under high vacuum after approximately 2 hours. This produced a 13.0 g yield or a 92.1% yield of the derivative. The NMR characterization data for the derivative is as follows. 1NMR (300 MHz, CDCl3): 0.88 (t, J=6.3, 6H, CH2CH3), 1.20-1.45 (m, 32H, CH2(CH2)8), 1.69-1.78 (m, 5H, OCH2CH2 & OH), 3.92 (t, J=6.6, 4H, OCH2), 4.61 (d, J=5.5, 2H, ArCH2OH), 6.37 (t, J=2.2, 1H, ArH), 6.48 (d, J=1.9, 2H, ArH). 13C NMR (75 MHZ, CDCl3): 14.23, 22.79, 26.13, 29.34, 29.44, 29.48, 29.68, 29.71, 32.00, 65.57, 68.13, 100.58, 105.10, 143.25, 160.60.

Provenance & Evidence