HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951602Generated: November 1, 2026
Hydrochloric Acid → 3-(4-Acetyl-2-methylphenyl)acrylic acid
https://huagongshe.com/reaction/1951602
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl 3-(4-acetyl-2-methylphenyl)-2-bromopropionate | HCID 86636689 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(4-Acetyl-2-methylphenyl)acrylic acid | HCID 69000452 | 34.5% |
Reaction Steps
The obtained methyl 3-(4-acetyl-2-methylphenyl)-2-bromopropionate (2.79 g, 9.33 mmol) was dissolved in methanol (80 mL). The solution was cooled to 5° C. Sodium methoxide (1.51 g, 27.98 mmol) was added to the solution. The mixture was stirred at room temperature for 20 minutes, refluxed for 1 hour, cooled to room temperature, and acidized with 1N hydrochloric acid. Water (50 mL) was added to the mixture. The mixture was extracted with chloroform. The organic layer was dried with anhydrous sodium sulfate. The solvent was removed under reduced pressure to give 657 mg of the desired compound as yellow crystalline product (yield 34%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404726B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-2777a7ee417c45a6bb069cf8a41faccc |
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| Source note | uspto-grants-2013_03 |
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