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(S)-1-methylpyrrolidin-3-yl (R)-2-cyclopentyl-2-hydroxy-2-phenylacetate synthesis

6synthesis methods
64471-47-2 Synthesis
Methyl (R)-(-)-cyclopentylmandelate

64471-47-2
20 suppliers
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(S)-1-methylpyrrolidin-3-yl (R)-2-cyclopentyl-2-hydroxy-2-phenylacetate

207856-85-7
18 suppliers
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Yield:207856-85-7 89.6%

Reaction Conditions:

Stage #1: (R)-α-phenyl-α-cyclopentyl-α-hydroxyacetate methyl ester;(3S)-1-methylpyrrolidin-3-olwith sodium in n-heptane at 110; for 3 h;
Stage #2: with water in n-heptane at 0;

References:

Wu;Wu;Mori;Buchwald;Bodor, Nicholas [Pharmazie,2008,vol. 63,# 3,p. 200 - 209] Location in patent:experimental part

13220-33-2 Synthesis
1-Methyl-3-pyrrolidinol

13220-33-2
313 suppliers
$11.00/1g

616866-21-8 Synthesis
(R)-(R)-1-methylpyrrolidin-3-yl 2-cyclopentyl-2-hydroxy-2-phenylacetate(WXC03446)

616866-21-8
24 suppliers
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(S)-1-methylpyrrolidin-3-yl (R)-2-cyclopentyl-2-hydroxy-2-phenylacetate

207856-85-7
18 suppliers
inquiry

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