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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379521Generated: October 30, 2026

Methyl acetoacetate → Methyl 3-oxo-7,11,15-trimethylhexadeca-6,10,14-trienoate

https://huagongshe.com/reaction/2379521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl acetoacetateHCID 7757—
ReactantSodium hydrideHCID 24758—
ReactantFarnesyl bromideHCID 550199—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductMethyl 3-oxo-7,11,15-trimethylhexadeca-6,10,14-trienoateHCID 54245426—

Reaction Conditions

Temperature0 °C

Reaction Steps

Methyl acetoacetate (225 μL, 2.1 mmol) was added dropwise to a stirred suspension of sodium hydride (50% oil suspension, prewashed with hexane) (100 mg, 2.1 mmol) in anhydrous THF (5 mL) at 0° C. under an Argon atmosphere. The resulting solution was stirred 15 minutes at 0° C. and then treated with a 1.6M solution (1.3 mL, 2.1 mmol) of n-butylithium in hexane over 2 minutes. The yellow solution was stirred 15 min at 0° C. and then treated dropwise with farnesyl bromide (545 μL, 2.0 mmol). The cloudy orange solution was stirred at 20° C. for 11/2 hours and then quenched by dropwise addition of saturated aqueous NH4Cl solution. The resulting mixture was diluted with ethyl acetate and washed with water, dried, filtered and evaporated to give the crude product which was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05362906
Source datasetuspto-grants-1994_11
ORD IDord-a5a8a985beb948b38bfd0eccdaaad963
Source noteuspto-grants-1994_11