HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599356Generated: October 30, 2026
Methyl vinyl ketone → HCID 10998092, compound
https://huagongshe.com/reaction/599356
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | 3,4-Dimethoxyaniline | HCID 22770 | — |
| Catalyst | Trichloroiron;hexahydrate | HCID 16211236 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 10998092 | HCID 10998092 | 38% |
Reaction Steps
The Reference Compound No. 1-1 was prepared following the method described in J. Org. Chem., 62, 568-577 (1997). Namely, iron (III) chloride hexahydrate (5.7 g, 21 mmol) and 3,4-dimethoxyaniline (3.1 g, 20 mmol) were added to acetic acid (60 mL), and then the mixture was stirred at 60° C. After all the solids were dissolved, methylvinylketone (1.8 mL, 22 mmol) was added dropwise for 5 minutes. Then the mixture was stirred at 140° C. for 1 hour, and allowed to cool down to room temperature, and the resulting solid was filtered off. Ethyl acetate (200 mL) was added to the solid, and the resulting organic solution was washed with 0.1N sodium hydroxide aqueous solution (200 mL) and brine (100 mL), and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the resulting solid was filtered off with diethyl ether to give 1.6 g of the title reference compound as a light brown solid (Yield: 38%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897774B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-396bff6153aa4faa90ab782c7bd4af6e |
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| Source note | uspto-grants-2011_03 |
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