
1-[4-(ALLYLOXY)PHENYL]ETHANONE synthesis
- Product Name:1-[4-(ALLYLOXY)PHENYL]ETHANONE
- CAS Number:2079-53-0
- Molecular formula:C11H12O2
- Molecular Weight:176.21

106-95-6
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99-93-4
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![1-[4-(ALLYLOXY)PHENYL]ETHANONE](/CAS/GIF/2079-53-0.gif)
2079-53-0
16 suppliers
$45.00/100mg
Yield:2079-53-0 100%
Reaction Conditions:
with potassium carbonate in acetone at 20;Reflux;
Steps:
153.153-a-1
Example 153; Preparation of 3-((4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-2-propylphenoxy)pyridin-2-yl) methyl)-5-methyl-5-(2-methyl-2,3-dihydrobenzofuran-5-yl)imidazolidine-2,4-dione; 153-a-1) Preparation of 1-(4-(allyloxy)phenyl)ethanone; 2-Hydroxyacetophenone (1.36 g, 10.0 mmol) was dissolved in acetone (50 mL). The resultant mixture was added with potassium carbonate (2.76 g, 20.0 mmol) and allylbromide (1.27 mL, 15.0 mmol) at room temperature and heated to reflux for 3 hours. The reaction solution was cooled to room temperature, added with ethyl acetate, and washed with water and brine. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. The obtained residue was purified using silica-gel column chromatography (n-hexane/ethyl acetate=10/1). 1-(4-(Allyloxy)phenyl)ethanone (1.76 g, 100%) was obtained as a colorless oil.1H-NMR (CDCl3) δ: 2.56 (3H, s), 4.60-4.62 (2H, m), 5.31-5.45 (2H, m), 6.00-6.09 (1H, m), 6.93-6.97 (2H, m), 7.92-7.95 (2H, m).
References:
US2010/48610,2010,A1 Location in patent:Page/Page column 85-86

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![1-[4-(ALLYLOXY)PHENYL]ETHANONE](/CAS/GIF/2079-53-0.gif)
2079-53-0
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$45.00/100mg

107-05-1
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$16.80/100ML

99-93-4
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![1-[4-(ALLYLOXY)PHENYL]ETHANONE](/CAS/GIF/2079-53-0.gif)
2079-53-0
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![1-[4-(2-PROPYNYLOXY)PHENYL]-1-ETHANONE](/CAS/GIF/34264-14-7.gif)
34264-14-7
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![1-[4-(ALLYLOXY)PHENYL]ETHANONE](/CAS/GIF/2079-53-0.gif)
2079-53-0
16 suppliers
$45.00/100mg

106-95-6
427 suppliers
$10.00/5g

99-93-4
887 suppliers
$5.00/25g
![1-[4-(ALLYLOXY)PHENYL]ETHANONE](/CAS/GIF/2079-53-0.gif)
2079-53-0
16 suppliers
$45.00/100mg

98-86-2
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$9.00/5g