HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221584Generated: November 2, 2026
4-Hydroxybenzaldehyde → Methyl 3-{4-[(4-formylphenoxy)methyl]-5-methyl-1,3-oxazol-2-yl}benzoate
https://huagongshe.com/reaction/2221584
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-(4-chloromethyl-5-methyl-1,3-oxazol-2-yl)benzoate | HCID 23076520 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-{4-[(4-formylphenoxy)methyl]-5-methyl-1,3-oxazol-2-yl}benzoate | HCID 86605721 | 94% |
Reaction Steps
A mixture of methyl 3-(4-chloromethyl-5-methyl-1,3-oxazol-2-yl)benzoate (2.0 g), 4-hydroxybenzaldehyde (0.87 g), potassium carbonate (0.98 g) and N,N-dimethylformamide (50 mL) was stirred at 90° C. for 2 hrs. Water was poured into the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated to give methyl 3-{4-[(4-formylphenoxy)methyl]-5-methyl-1,3-oxazol-2-yl}benzoate as colorless crystals (2.33 g, yield 94%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 103-104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07368578B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-e0441eb400af4b4d9fb167e7c49f299a |
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| Source note | uspto-grants-2008_05 |
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