HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357359Generated: October 26, 2026
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 2,4,5-Trimethoxy phenyl propionone
https://huagongshe.com/reaction/1357359
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | gamma-Asarone | HCID 636750 | — |
| Reactant | Asarone | HCID 636822 | — |
| Reactant | Beta-Asarone | HCID 5281758 | — |
| Product | 2,4,5-Trimethoxy phenyl propionone | HCID 86759060 | — |
Reaction Steps
The present invention relates to a process for the preparation of high purity and yield α-asarone, trans 2,4,5-trimethoxy cinnamaldehyde, 2,4,5-trimethoxy-phenyl propionone, from β-asarone or β-asarone rich Acorus calamus oil containing α and γ-asarone by hydrogenating, followed by treatment with DDQ with or without solid support of silica gel or alumina in dry organic solvent and α-asarone can also be obtained by treating the hydrogenated product of β-asarone or β-asarone rich Acorus calamus with DDQ in an aqueous organic solvent to obtain an intermediate 2,4,5-trimethoxy phenyl propionone, which in turn is reduced with sodiumborohydride to obtain the corresponding 2,4,5-trimethoxy-phenyl propanol and followed by final treatment with a dehydrating agent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06590127B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-8567a0abc19144ffa6394f8221dd38be |
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| Source note | uspto-grants-2003_07 |
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