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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486840Generated: October 30, 2026

Hydrochloric Acid → 6-(3-Chloro-2-oxopropyl)-2,2-dimethyl-2H,4H-1,3-dioxin-4-one

https://huagongshe.com/reaction/486840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloroacetyl chlorideHCID 6577—
Reactant2,2,6-Trimethyl-4H-1,3-dioxin-4-oneHCID 79368—
ReactantLithium diisopropylamideHCID 2724682—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product6-(3-Chloro-2-oxopropyl)-2,2-dimethyl-2H,4H-1,3-dioxin-4-oneHCID 1494482869%

Reaction Steps

In an argon gas stream, 20.6 ml of n-butyl lithium (1.6M solution in hexane) were added to 60 ml of an ether solution containing 3.53 g (0.033 mol) of diisopropylamine at -20° C. to form LDA. After stirring for 30 minutes, a mixture of 4.26 g (0.03 mol) of 2,2-dimethyl-6-methyl-1,3-dioxin-4-one and 60 ml of ether as well as 60 ml of an ether solution containing 1.69 g (0.015 mol) of chloroacetyl chloride were added to LDA. After the temperature was gradually returned to room temperature, 10% hydrochloric acid was added thereto to neutralize the solution, and extraction was then carried out with ether. The resultant organic layer was dried over anhydrous magnesium sulfate. Next, the solvent was distilled off, and the residue was then subjected to column chromatography (an eluent of hexane:ethyl acetate=4:1), thereby obtaining 2.26 g (yield 69%) of 2,2-dimethyl-6-(3-chloro-2-oxopropyl)-1,3-dioxin-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292891
Source datasetuspto-grants-1994_03
ORD IDord-a65d247b196c473c9f4225b28a2ea62e
Source noteuspto-grants-1994_03