![](/CAS/GIF/154825-95-3.gif)
4-[4-[4-(HydroxydiphenylMethyl)-1-piperidinyl]-1-butyn-1-yl]-α,α-diMethyl-benzeneacetic Acid Methyl Ester synthesis
- Product Name:4-[4-[4-(HydroxydiphenylMethyl)-1-piperidinyl]-1-butyn-1-yl]-α,α-diMethyl-benzeneacetic Acid Methyl Ester
- CAS Number:154825-95-3
- Molecular formula:C33H37NO3
- Molecular Weight:495.65
![methyl 2-(4-(4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)but-1-ynyl)phenyl)-2-methyl propionate oxalate](/CAS/20180601/GIF/1352802-40-4.gif)
1352802-40-4
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![4-[4-[4-(HydroxydiphenylMethyl)-1-piperidinyl]-1-butyn-1-yl]-α,α-diMethyl-benzeneacetic Acid Methyl Ester](/CAS/GIF/154825-95-3.gif)
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Yield:154825-95-3 99.7%
Reaction Conditions:
with ammonia in water;toluene; pH=9;
Steps:
2
In a 5L four-neck flask equipped with mechanical stirrer, a thermometer, a condenser and a dropping funnel, toluene (2L), water ( 1 L) and methyl 2-(4-(4-(4- (hydroxydiphenylmethyl)piperidin-l -yl)but-l -ynyl)phenyl)-2-methylpropionate oxalate (II) (403 g, 688 mmol) were added. Under stirring, a water solution of ammonia (24%, 100 g, 1410 mmol) was added until pH 9 was reached. The phases were separated, the organic phase was washed with water (500 mL) and concentrated under vacuum to obtain 340 g of (III). Yield: 99.7%.
References:
WO2011/158262,2011,A1 Location in patent:Page/Page column 12
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1798-50-1
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$24.73/250mgs:
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154825-94-2
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![METHYL 2-(4-BROMOPHENYL)-2,2-DIMETHYLACETATE](/CAS/GIF/154825-97-5.gif)
154825-97-5
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![4-[4-[4-(HydroxydiphenylMethyl)-1-piperidinyl]-1-butyn-1-yl]-α,α-diMethyl-benzeneacetic Acid Methyl Ester](/CAS/GIF/154825-95-3.gif)
154825-95-3
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