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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481866Generated: October 31, 2026

Methyl acetoacetate → HCID 54704707, compound

https://huagongshe.com/reaction/481866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl acetoacetateHCID 7757—
ReactantSodium hydrideHCID 24758—
ReactantHCID 69836888HCID 69836888—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 54704707HCID 54704707—
ProductHCID 69836888HCID 69836888—

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 in 50 mL of tetrahydrofuran and 25 mmol of 4-benzoylbutyric acid sodium salt in 100 mL of tetrahydrofuran. 4-Benzoylbutyric acid sodium salt was prepared by reacting the acid (25 mmol) with hexane washed NaH (17.5 mmol) in tetrahydrofuran at 0° C. for 25 minutes. The crude product was flash chromatographed using CH2Cl2 /MeOH/CH3CO2H (99/1/0.1-97.5/2.5/0.1) to give a solid which was recrystallized from ethyl acetate (m.p. 134°-137° C.). 1H NMR (DMSO-d6) δ1.1-1.2 (m, 1H), 1.4-1.6 (m, 1H), 1.8-2.0 (m, 2H), 2.0-2.2 (m, 2H), 2.9 (ABq, 2H), 4.85 (s, 1H), 7.2-7.4 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789440
Source datasetuspto-grants-1998_08
ORD IDord-479bbe2427d9459bb8e25c79451197dc
Source noteuspto-grants-1998_08