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(S)-3-(4-(2-(4-fluorophenyl)-5,5-diMethyl-1,3-dioxan-2-yl)butanoyl)-4-phenyloxazolidin-2-one synthesis
- Product Name:(S)-3-(4-(2-(4-fluorophenyl)-5,5-diMethyl-1,3-dioxan-2-yl)butanoyl)-4-phenyloxazolidin-2-one
- CAS Number:953805-20-4
- Molecular formula:C25H28FNO5
- Molecular Weight:441.49
![2,2-Dimethyl-1,3-propanediol](/CAS/GIF/126-30-7.gif)
126-30-7
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![(4S)-3-[5-(4-Fluorophenyl)-1,5-dioxopenyl]-4-phenyl-2-oxazolidinone](/CAS/GIF/189028-93-1.gif)
189028-93-1
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![(S)-3-(4-(2-(4-fluorophenyl)-5,5-diMethyl-1,3-dioxan-2-yl)butanoyl)-4-phenyloxazolidin-2-one](/CAS/20150408/GIF/953805-20-4.gif)
953805-20-4
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Yield:953805-20-4 89%
Reaction Conditions:
with phosphorus pentoxide;sulfuric acid in dichloromethane; for 5 h;Reflux;
Steps:
3 Synthesis of Compound III (wherein R1 = R2 = CH3)
Compound II (35.5 g, 0.1 mol) was added to a 500 ml three-necked flask, 200 ml of dichloromethane, Then, 2,2-dimethyl-1,3-propanediol (15.6 g, 0.15 mol), phosphorus pentoxide (14.2 g, 01 mol) and concentrated sulfuric acid (0.98 g, 0.01 mol) Reflux reaction for 5 hours, After the reaction, the ice bath cools down, And then adjusted to pH 7 with saturated aqueous sodium bicarbonate solution, Static stratification, Dichloromethane layer washed, Dried over anhydrous sodium sulfate, Concentrated to dry, To give 41.2 g of a white solid compound III, Yield 89%.
References:
CN106397292,2017,A Location in patent:Paragraph 0053; 0089; 0090
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![(S)-3-(4-(2-(4-fluorophenyl)-5,5-diMethyl-1,3-dioxan-2-yl)butanoyl)-4-phenyloxazolidin-2-one](/CAS/20150408/GIF/953805-20-4.gif)
953805-20-4
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149437-76-3
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![(S)-3-(4-(2-(4-fluorophenyl)-5,5-diMethyl-1,3-dioxan-2-yl)butanoyl)-4-phenyloxazolidin-2-one](/CAS/20150408/GIF/953805-20-4.gif)
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462-06-6
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![(S)-3-(4-(2-(4-fluorophenyl)-5,5-diMethyl-1,3-dioxan-2-yl)butanoyl)-4-phenyloxazolidin-2-one](/CAS/20150408/GIF/953805-20-4.gif)
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108-55-4
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![(S)-3-(4-(2-(4-fluorophenyl)-5,5-diMethyl-1,3-dioxan-2-yl)butanoyl)-4-phenyloxazolidin-2-one](/CAS/20150408/GIF/953805-20-4.gif)
953805-20-4
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