Reaction #166175

Reaction equation

sodium tert-butoxide

phosphine

4-chlorotoluene

morpholine

→

4-Tolylmorpholine

Solvents

acetonitrile

CH2Cl2

dioxane

Conditions

Workup

1. 1
   OtherIn a nitrogen-atmosphere glovebox, a microwave vial equipped with a magnetic stir bar
2. 2
   OtherThe vial was sealed with a crimp top
3. 3
   Otherthe vial was removed from the heating block
4. 4
   Temperaturecooled to room temperature
5. 5
   Otherreaction
6. 6
   Filtrationfiltering into a round-bottom flask
7. 7
   WashThe vial was rinsed with CH2Cl2 (5 mL)
8. 8
   Washby washing of the filter cake with CH2Cl2 (2 mL)
9. 9
   OtherThe volatiles were removed on a rotary evaporator
10. 10
    Concentrationthe crude concentrate
11. 11
    Otherwas purified by silica gel column chromatography (25 g silica gel, 85:15 heptane:ethyl acetate)
12. 12
    OtherThe purified product was isolated as a beige solid

Procedure

In a nitrogen-atmosphere glovebox, a microwave vial equipped with a magnetic stir bar was charged with sodium tert-butoxide (56.9 mg, 0.592 mmol, 1.5 equivalents), tris(dibenzylideneacetone)dipalladium(0) (Pd2dba3) (3.62 mg, 0.00395 mmol, 0.01 equivalents), phosphine ligand (0.00869 mmol, 0.022 equivalents) and dioxane (0.79 mL). To the slurry was added 4-chlorotoluene (47 μL, 0.395 mmol, 1 equivalents) and morpholine (42 μL, 0.474 mmol, 1.2 equivalents). The vial was sealed with a crimp top and stirred at 100° C. After 14 hours, the vial was removed from the heating block, cooled to room temperature and brought out of the glovebox. To assay the crude reaction, an aliquot (7 μL) was taken and diluted in acetonitrile (1.5 mL), then injected onto an HPLC instrument. For isolation purposes, the reaction solution was worked up by diluting with CH2Cl2 (2 mL) and filtering into a round-bottom flask. The vial was rinsed with CH2Cl2 (5 mL), followed by washing of the filter cake with CH2Cl2 (2 mL). The volatiles were removed on a rotary evaporator and the crude concentrate was purified by silica gel column chromatography (25 g silica gel, 85:15 heptane:ethyl acetate). The purified product was isolated as a beige solid. 1H NMR (400 MHz, CDCl3) δ ppm 7.10 (d, J=8.2 Hz, 1H), 6.88-6.81 (m, 2H), 3.87 (dd, J=5.7, 3.9 Hz, 4H), 3.15-3.09 (m, 4H), 2.29 (s, 3H).

Source