HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350009Generated: October 26, 2026
4-Hydroxybenzaldehyde → 4-(5-Methyl-2-phenyl-4-thiazolylmethoxy)benzaldehyde
https://huagongshe.com/reaction/350009
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Thiazole, 4-(chloromethyl)-5-methyl-2-phenyl- | HCID 12794636 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(5-Methyl-2-phenyl-4-thiazolylmethoxy)benzaldehyde | HCID 23025085 | 93% |
Reaction Steps
A mixture of 4-chloromethyl-5-methyl-2-phenylthiazole (5.40 g), 4-hydroxybenzaldehyde (2.91 g), anhydrous potassium carbonate (4.95 g) and N,N-dimethylformamide (50 ml) was stirred at 80° C. for 3 hours. The reaction mixture was poured into water, the precipitated solid was collected by filtration, and air-dried to obtain crystals of 4-(5-methyl-2-phenyl-4-thiazolylmethoxy)benzaldehyde (6.85 g, yield 93%). This was recrystallized from ethyl acetate-hexane to obtain colorless prisms. Melting point: 118–119° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07179823B1 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-549e03a5026d4423a08f028974523830 |
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| Source note | uspto-grants-2007_02 |
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