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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533694Generated: October 25, 2026

4-Oxo-undecanoyl Chloride → HCID 54155424, compound

https://huagongshe.com/reaction/1533694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Oxo-undecanoyl ChlorideHCID 22990500—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantAcetic Acid 3-(4-tert-butyl-phenyl)-2-methyl-propenyl EsterHCID 53757095—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54155424HCID 5415542437.4%

Reaction Steps

A solution of 43.79 g acetic acid 3-(4-tert-butyl-phenyl)-2-methyl-propenyl ester in 200 ml of THF was cooled to −70° C. A solution of 27.16 g potassium-tert-butoxide in 200 ml of THF was added at −70° C. during 20 min. and the resulting reaction mixture was stirred for 90 min. at the same temperature. Then a solution of 53.00 g 4-oxo-undecanoyl chloride in 200 ml of THF was dropped in and the reaction mixture was stirred for another 2.5 hours at −70° C. Then the reaction mixture was diluted with ether, washed with saturated NaHCO3 and brine. The organic phase was dried, filtered and evaporated to dryness. The residue was thin-layer distilled and purified by chromatography to yield 25.73 g of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207857B1
Source datasetuspto-grants-2001_03
ORD IDord-aa1572beb9224bd982ab75748bd6b4b4
Source noteuspto-grants-2001_03