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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481863Generated: October 30, 2026

Methyl acetoacetate → 2-cyclopentyl-1-phenyl-ethanone

https://huagongshe.com/reaction/481863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl acetoacetateHCID 7757—
ReactantSodium hydrideHCID 24758—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-cyclopentyl-1-phenyl-ethanoneHCID 12217744—
ReactantButyllithiumHCID 178418339—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-cyclopentyl-1-phenyl-ethanoneHCID 12217744—
ProductHCID 54690707HCID 54690707—

Reaction Steps

The title compound was prepared as described in General Method 1 using 25 mmol of methyl acetoacetate, 27.5 mmol of NaH 60% dispersion in oil, 26.25 mmol of 1.6M n-butyl lithium in hexane, 25 mmol of 2-cyclopentyl-1-phenyl-ethanone and 70 mL of tetrahydrofuran. 2-Cyclopentyl-1-phenyl-ethanone was prepared by reacting the appropriate acid chloride with AlCl3 in benzene as described by Vogel in Practical Organic Chemistry 1978, 770-775. Upon concentrating the reaction, a solid precipitated out which was recrystallized from ethyl acetate (m.p. 158°-160° C.). 1H NMR (DMSO-d6) δ0.8-0.9 (m, 1H), 1.0-1.1 (m, 1H), 1.2-1.8 (m, 7H), 1.9-2.1 (m, 2H), 2.9 (ABq, 2H), 4.8 (s, 1H), 7.2-7.4 (m, 5H), 11.3 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789440
Source datasetuspto-grants-1998_08
ORD IDord-3a003170b5834fabbc90ab5c1dae4ed4
Source noteuspto-grants-1998_08