HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436879Generated: October 27, 2026
Hydrochloric Acid → Methyl 11-methoxy-7,11-dimethyl-3-oxo-6-dodecenoate
https://huagongshe.com/reaction/436879
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methylcarbonate | HCID 4585885 | — |
| Reactant | 10-Methoxy-6,10-dimethyl-5-undecene-2-one | HCID 53966525 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 11-methoxy-7,11-dimethyl-3-oxo-6-dodecenoate | HCID 54124623 | — |
Reaction Steps
A mixture of 900 mg of the product from Step B, 1 ml of methyl carbonate and 15 ml of dimethylformamide was heated to 40° C. and 360 mg of sodium hydride in a 50% oil suspension were added thereto portion wise and the mixture was stirred for 6 hours at room temperature. The mixture was poured into an aqueous hydrochloric acid solution and was extracted with petroleum ether (b.p.= 40°-75° C.). The extracts were washed with water, dried over sodium sulfate and evaporated to dryness. The residue was chromatographed over silica and was eluted with a 7-3 petroleum ether-ethyl ether mixture to obtain 374 mg of methyl 11-methoxy-7,11-dimethyl-3-oxo-6-dodecenoate in the form of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04028386 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-26cefb315ec441a08003a475254ec5a2 |
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| Source note | uspto-grants-1977_06 |
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