HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740923Generated: October 30, 2026
3-Hydroxybenzaldehyde → 3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzaldehyde
https://huagongshe.com/reaction/1740923
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloromethyl-5-methyl-2-phenyloxazole | HCID 18546173 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzaldehyde | HCID 10708843 | 91.1% |
Reaction Steps
A mixture of 2-chloromethyl-5-methyl-2-phenyloxazole (20.8 g), 3-hydroxybenzaldehyde (12.2 g), potassium carbonate (27.6 g) and N,N-dimethylformamide (DMF) (200 ml) was heated at 90° C. for 2 hours. The reaction mixture was poured into water, and subjected to extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried over magnesium sulfate (MgSO4). The solvent was distilled off, whereby 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzaldehyde (26.5 g, 90%) was obtained. Recrystallization from ethanol gave colorless prisms. Melting point: 67-68° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05972970 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-bc5a5ac3785c4769a94956fe8db872d9 |
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| Source note | uspto-grants-1999_10 |
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