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Chemical Structure| 87326-00-9 Chemical Structure| 87326-00-9

Structure of 87326-00-9

Chemical Structure| 87326-00-9

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Product Details of [ 87326-00-9 ]

CAS No. :87326-00-9
Formula : C10H16O4
M.W : 200.23
SMILES Code : O=C(C1(OC2CCCCO2)CC1)OC

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Application In Synthesis of [ 87326-00-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 87326-00-9 ]

[ 87326-00-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 110-87-2 ]
  • [ 33689-29-1 ]
  • [ 87326-00-9 ]
YieldReaction ConditionsOperation in experiment
86% pyridinium p-toluenesulfonate; In dichloromethane; at 25℃; for 3h; Hydroxy-cyclopropanecarboxylic acid methyl ester (5.07 g, 43.71 mmol) was dissolved in methylene chloride (75 mL) and 3,4-dihydro-2H-pyran (3.86 g, 45.90 mmol) was added followed by pyridinium-p-toluene-sulfonic acid (1.10 g, 4.37 mmol). The reaction stirred at 25 C. for 3 h. The reaction was concentrated in vacuo to give a clear oil. The oil was dissolved in diethyl ether (75 mL), washed with saturated aqueous brine solution (25 mL), dried over sodium sulfate and concentrated in vacuo to an oil. The oil was passed through a plug of silica gel (Merck silica gel 60, 40-63 mum; 100% ethyl acetate) to afford 1-(tetrahydro-pyran-2-yloxy)-cyclopropanecarboxylic acid methyl ester (7.49 g, 86%) as a clear oil: H1-NMR (400 MHz, CDCl3) delta 1.14-1.42 (4H, m), 1.88-3.46 (6H, m), 3.46-3.54 (1H, m), 3.70-3.72 (3H, m), 3.82-3.90 (1H, m), 4.81-4.96 (1H, m).
60% With pyridinium p-toluenesulfonate; In dichloromethane; at 23℃; for 16h;Sealed tube; Methyl 1-hydroxycyclopropanecarboxylate (1.12 g, 9.65 mmol) was dissolved in DCM (15 mL) and3,4-dihydro-2H-pyran (0.9 mL, 10.13 mmol) was added, followed by pyridmnium p-toluenesulfonate (0.242 g, 0.965 mmol). The colorless solution was stirred at RT in a sealed vessel for 16 h. The reaction mixture was concentrated in vacuo. The white suspension was partitioned between brine (20 mL) and Et20 (20 mL) and the layers were separated. The organic layer was washed with brine (2x 5mL) and dried on Na2504 before concentration in vacuo. The product was purified using CC (silica, gradient heptane/EtOAc, 1:0-. 8:2)to give the desired product (1.16 g, 60%) as a colorless oil.
 

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