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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486845Generated: October 30, 2026

Hydrochloric Acid → HCID 14559528, compound

https://huagongshe.com/reaction/486845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl vinyl ketoneHCID 6570—
ReactantHexamethylphosphoramideHCID 12679—
Reactant2,2,6-Trimethyl-4H-1,3-dioxin-4-oneHCID 79368—
SolventDiethyl EtherHCID 3283—
ProductHCID 14559528HCID 1455952849.6%

Reaction Conditions

Temperature-78 °C

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, the solution was cooled to -78° C., and 10.4 ml (0.06 mol) of HMPA were added thereto, followed by stirring for 15 minutes. Afterward, 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 2.1 g (0.03 mol) of methyl vinyl ketone were added to the solution. 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 used solvent was distilled off, and the residue was then subjected to column chromatography (an eluent of hexane:ethyl acetate=4:1), thereby obtaining 3.16 g of 2,2-dimethyl-6-(4-oxopentyl)-1,3-dioxin-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292891
Source datasetuspto-grants-1994_03
ORD IDord-bfc07f57378f4079a5be399613d324e5
Source noteuspto-grants-1994_03