3-CYCLOPENTYL-3-OXO-PROPIONIC ACID ETHYL ESTER

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Products Intro: Product Name:3-CYCLOPENTYL-3-OXO-PROPIONIC ACID ETHYL ESTER
CAS:24922-00-7
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3-CYCLOPENTYL-3-OXO-PROPIONIC ACID ETHYL ESTER manufacturers

3-CYCLOPENTYL-3-OXO-PROPIONIC ACID ETHYL ESTER Basic information
Uses
Product Name:3-CYCLOPENTYL-3-OXO-PROPIONIC ACID ETHYL ESTER
Synonyms:3-CYCLOPENTYL-3-OXO-PROPIONIC ACID ETHYL ESTER;Ethyl 3-cyclopentyl-3-oxopropionate;Cyclopentanepropanoicacid, b-oxo-, ethyl ester;Cyclopentanepropanoicacid, b-oxo;Cyclopentanepropanoic acid, β-oxo-, ethyl ester;ETHYL 3-CYCLOPENTYL-3-OXOPROPANOATE
CAS:24922-00-7
MF:C10H16O3
MW:184.23
EINECS:
Product Categories:
Mol File:24922-00-7.mol
3-CYCLOPENTYL-3-OXO-PROPIONIC ACID ETHYL ESTER Structure
3-CYCLOPENTYL-3-OXO-PROPIONIC ACID ETHYL ESTER Chemical Properties
Boiling point 91-94 °C(Press: 1.8 Torr)
density 1.065±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka10.51±0.20(Predicted)
AppearanceColorless to light yellow Liquid
Safety Information
HS Code 2918999090
MSDS Information
3-CYCLOPENTYL-3-OXO-PROPIONIC ACID ETHYL ESTER Usage And Synthesis
UsesEthyl 3-cyclopentyl-3-oxopropionate can be used as a pharmaceutical synthesis intermediate.
Synthesis
Cyclopentanecarbonyl chloride

4524-93-0

3-CYCLOPENTYL-3-OXO-PROPIONIC ACID ETHYL ESTER

24922-00-7

6a) A hexane solution of 2.4 M n-butyllithium (92.0 mL, 230 mmol) was slowly added dropwise to a solution containing monoethyl malonate (13.6 mL, 115 mmol) and a catalytic amount of 2,2'-bipyridine at -55 to -65 °C. After the dropwise addition, cyclopentanecarbonyl chloride (7.0 mL, 58 mmol) was added in batches. The reaction mixture was gradually warmed to room temperature with stirring and subsequently poured into a mixture of 1N aqueous hydrochloric acid solution and ether. The organic layer was separated, washed three times with saturated sodium bicarbonate solution, dried over anhydrous magnesium sulfate, concentrated and then purified by silica gel column chromatography (eluent: 0-5% ethyl acetate in hexane solution with gradient elution) to afford ethyl 3-cyclopentyl-3-oxopropanoate (9.50 g, 89% yield).1H-NMR (400 MHz, DMSO-d6) δ 4.06 (q, J = 7 Hz. 2H), 3.60 (s, 2H), 2.99-2.91 (m, 1H), 1.78-1.47 (m, 8H), 1.15 (t, J = 7 Hz, 3H).

References[1] Patent: US2008/96921, 2008, A1. Location in patent: Page/Page column 42
[2] Journal of Medicinal Chemistry, 1998, vol. 41, # 17, p. 3186 - 3201
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