反应 #1256705

反应方程式

4-bromo-3,5-dimethyl-pyridine 1-oxide

2

4-methoxy-2,6-dimethylphenylboronic acid

dicyclohexyl-(2-phenanthren-9-yl-phenyl)-phosphane

K3PO4

→

title compound

收率 1.8%

4-(4-methoxy-2,6-dimethyl-phenyl)-3,5-dimethyl-pyridin-1-ol

收率 1.8%

反应条件

后处理

1. 1
   其他The Schlenk tube was next evacuated
2. 2
   其他Then, degassed dry toluene (100 mL)
3. 3
   workup.ADDITIONwas added via syringe under N2
4. 4
   其他The Schlenk tube was sealed
5. 5
   温度The reaction mixture was subsequently cooled to room temperature
6. 6
   workup.ADDITIONdiluted with methylene chloride (500 mL)
7. 7
   过滤filtered
8. 8
   浓缩concentrated in vacuo
9. 9
   其他to stand at room temperature until the colorless crystalline product
10. 10
    其他separated from the liquid
11. 11
    过滤The solid was then collected by filtration
12. 12
    其他The filtrate was purified by flash chromatography
13. 13
    洗涤eluting with 95:5 CHCl3

实验过程

A flame-dried sealable Schlenk tube was charged with 4-bromo-3,5-dimethyl-pyridine 1-oxide (1; 10.1 g, 50.0 mmol), 2 (18.0 g, 100 mmol), Pd2(dba)3 (0.915 g, 1.00 mmol), dicyclohexyl-(2-phenanthren-9-yl-phenyl)-phosphane (1.8 g, 4.0 mmol), and K3PO4 (31.9 g, 150 mmol). The Schlenk tube was next evacuated and backfilled with N2. Then, degassed dry toluene (100 mL) was added via syringe under N2. The Schlenk tube was sealed, and the mixture was stirred at 120° C. for 48 h. The reaction mixture was subsequently cooled to room temperature, diluted with methylene chloride (500 mL), filtered, and concentrated in vacuo. The resulting dark brown oil was allowed to stand at room temperature until the colorless crystalline product separated from the liquid. The solid was then collected by filtration and identified as the pure title compound (6.55 g). The filtrate was purified by flash chromatography eluting with 95:5 CHCl3: methanol to afford an additional 0.23 g of the title compound. The combined yield was 6.78 g (53%): mp 194-195° C.; 1H NMR (400 MHz, CD2Cl2): δ 7.990 (s, 2H), 6.705 (s, 2H), 3.798 (s, 3H), 1.892 (s, 6H), 1.842 (s, 6H); 13C NMR (125 MHz, CD2Cl2): δ 159.771, 139.578, 137.663, 137.187, 135.775, 128.289, 113.709, 55.605, 20.198, 17.087; MS (ESI): m/z 258.4 [(M+H)+, 100]; Anal. Calcd. For C16H19NO2: C, 74.68; H, 7.44; N, 5.44. Found: C, 74.54; H, 7.40; N, 5.51.

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