HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486845Generated: October 30, 2026
Hydrochloric Acid → HCID 14559528, compound
https://huagongshe.com/reaction/486845
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | 2,2,6-Trimethyl-4H-1,3-dioxin-4-one | HCID 79368 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 14559528 | HCID 14559528 | 49.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292891 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-bfc07f57378f4079a5be399613d324e5 |
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| Source note | uspto-grants-1994_03 |
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