HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217619Generated: October 31, 2026
Hydroxyphenylacetic acid → 2-(4-Acetoxyphenyl)-3-p-tolylacrylic acid
https://huagongshe.com/reaction/2217619
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxyphenylacetic acid | HCID 127 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-Acetoxyphenyl)-3-p-tolylacrylic acid | HCID 68794337 | 68.1% |
Reaction Steps
To a mixture of (4-hydroxyphenyl)-acetic acid (18.3 g, 120.3 mmol) and 4-methylbenzaldehyde (12.0 g, 100 mmol) in 250 mL acetic anhydride was added potassium carbonate (11.9 g, 121.2 mmol). The reaction mixture was stirred at 80° C. for 16 h before it was cooled to room temperature. To the mixture was added 100 mL H2O, 5% HCl in water to pH 1 and 200 mL ethyl acetate. The mixture was then heated to 80° C. until all ethyl acetate was evaporated. The precipitate was filtered and washed with water and hexane. The filter cake was recrystallized out of toluene, filtered, washed with hexane and dried under vacuum to yield a pale yellow powder (20.16 g, 68.1%). 1H NMR (400 MHz, DMSO-d6) δ 12.62 (br s, 1H), 7.74 (s, 1H), 7.19 (d, J=8.8 Hz, 2H), 7.13 (d, J=8.8 Hz, 2H), 7.01 (d, J=8.0 Hz, 2H), 6.94 (d, J=8.4 Hz, 2H), 2.29 (s, 3H), 2.23 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07407978B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-565e9dba8fe449ddab2ad8063780be6d |
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| Source note | uspto-grants-2008_08 |
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