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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779406Generated: October 26, 2026

Sodium hydride → Ethyl 2-(3-undecylphenoxy)-3-oxopentanoate

https://huagongshe.com/reaction/1779406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-chloro-3-oxopentanoateHCID 12923424—
Reactant3-UndecylphenolHCID 23274807—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductEthyl 2-(3-undecylphenoxy)-3-oxopentanoateHCID 1995550881.4%

Reaction Steps

A mixture of 7.0 grams (0.028 mole) of 3-undecylphenol (prepared in Steps A-C of this Example).and 1.1 grams (0.028 mole) of 60% sodium hydride (in mineral oil) in 100 mL of toluene was stirred for about 20 minutes, and 4.2 grams (0.028 mole) of ethyl 2-chloro-3-oxopentanoate (prepared in Step D of this example) was added dropwise during about a 12 minute period. Upon completion of addition, the reaction mixture was heated to reflux, where it was stirred for about 6.5 hours. After this time, the reaction mixture was allowed to cool to ambient temperature, where it stood for about 16 hours. The reaction mixture was then taken up in 50 mL of water and 5 mL of acetic acid. The mixture was washed with an additional 50 mL of water and then with 25 mL of an aqueous solution saturated with sodium chloride. The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 8.9 grams of ethyl 2-(3-undecylphenoxy)-3-oxopentanoate. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627189
Source datasetuspto-grants-1997_05
ORD IDord-cbb9e0abed2b475daf994a28b87aff3c
Source noteuspto-grants-1997_05