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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481862Generated: October 31, 2026

Methyl acetoacetate → 5-Methyl-1-phenylhexan-1-one

https://huagongshe.com/reaction/481862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl acetoacetateHCID 7757—
ReactantSodium hydrideHCID 24758—
Reactant5-Methyl-1-phenylhexan-1-oneHCID 570692—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantButyllithiumHCID 178418339—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-Methyl-1-phenylhexan-1-oneHCID 570692—
ProductHCID 54703398HCID 54703398—

Reaction Steps

The title compound was prepared as described in General Method 1 using 14.2 mmol of methyl acetoacetate, 15.6 mmol of NaH 60% dispersion in oil, 14.9 mmol of 1.6M n-butyl lithium in hexane, 14.2 mmol of isoheptanophenone and 50 mL of tetrahydrofuran. Isoheptanophenone 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. 124°-125° C.). 1H NMR (CDCl3) δ0.80 (d,d, 6H), 1.1-1.2 (m, 2H), 1.15-1.40 (m, 2H), 1.4-1.5 (m, 1H), 1.9-2.0 (m, 2H), 2.88 (d, 1H), 2.9 (d, 1H), 3.2 (d, 1H), 3.3 (d, 1H), 7.2-7.5 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789440
Source datasetuspto-grants-1998_08
ORD IDord-fb91f7de8e7645ae8852081de0504c26
Source noteuspto-grants-1998_08