An Efficient Copper-Catalyzed Etherification of Aryl Halides

Abstract

An efficient and mild copper-catalyzed ether formation from aryl halides and aliphatic alcohols has been developed. The key to the successful coupling is the use of lithium alkoxide, directly or in situ generated by lithium tert-butoxide, and the corresponding alcohol as solvent.

Key words

ligand-free - copper - etherification - aryl halides

References and Notes

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• 13 In the case of NaOt-Bu, toluene is detected as the major product from reduction of 4-bromotoluene. Bacon RG. Ressison SC. J. Chem. Soc. C  1969,  312 

10

A multikilogram process has been successfully carried out by us based on this protocol.

11

In our original process for the particular drug candidate, the very expensive 3,4,7,8-tetramethyl-1,10-phenanathroline (20 mol%, MW = 236.3. $63.9/g, from Aldrich) was used as ligand.

12

For the consideration of less stable substrate, intead of 110 ˚C as the original literature reported (ref. 6k), 100 ˚C was chosen for screening purpose.

14

Cu(II) salts were found slightly less effective.

15

The presence of other functional groups such as ester, carboxylic acid, nitro, and cyano were not successful under this protocol.

16

General Procedure for the Etherification of Arylbromides
To a 10 mL seal tube were charged alcohol (2.0 mL) and LiOt-Bu (480 mg, 6.0 mmol). The resulting suspension was stirred at r.t. for 5 min to form a clear solution. Arylbromide (2.0 mmol) and CuI (38 mg, 0.2 mmol) were added to the above solution. The mixture was stirred at r.t. for 5 min to form a nearly clear solution which was sealed and stirred at 80-110 ˚C for 18-28 h. The reaction was cooled to r.t. and quenched with AcOH (pH = 7-8) and diluted with CH₂Cl₂. The mixture was washed with H₂O (2 × 5 mL) and solvent removed. The crude residue was purified by silica gel column chromatography to give the desired product. The identity and purity of the products are confirmed by ^¹H NMR, ^¹³C NMR, and HRMS spectroscopic analysis.
5-(Pentyloxy)pyrimidin-2-ol (Table 2, Entry 8)
Off-white solid. ^¹H NMR (400 MHz, CDCl₃): δ = 8.04 (s, 2 H), 3.86 (t, J = 8 Hz, 2 H), 1.77 (m, 2 H), 1.40-1.45 (m, 4 H), 0.94 (t, J = 8 Hz, 3 H) ppm. ^¹³C NMR (100 MHz, CDCl₃):
δ = 157.9, 144.8, 142.2, 70.5, 28.7, 28.0, 22.4, 14.0 ppm. HRMS: m/z calcd for C₉H₁₄N₂O₂: 182.1055; found: 182.1053.
3-(2-Methoxyethoxy)pyridine (Table 2, Entry 9)
Colorless oil. ^¹H NMR (400 MHz, CDCl₃): δ = 8.35 (s, 1 H), 8.23 (m, 1 H), 7.23 (m, 2 H), 4.17 (t, J = 4 Hz, 2 H), 3.77
(t, J = 4 Hz, 2 H), 3.46 (s, 3 H) ppm. ^¹³C NMR (100 MHz, CDCl₃): δ = 155.0, 142.4, 138.0,. 123.8, 121.4, 70.9, 67.7, 59.3 ppm. HRMS: m/z calcd for C₈H₁₁NO₂: 153.0790; found: 153.0785.