HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299702Generated: October 26, 2026
Dimethylformamide → 3-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)phenyl]propanol
https://huagongshe.com/reaction/2299702
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(4-Hydroxyphenyl)propanol | HCID 82452 | — |
| Reactant | 4-(Chloromethyl)-5-methyl-2-phenyl-1,3-oxazole | HCID 9794289 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)phenyl]propanol | HCID 10925353 | 84% |
Reaction Steps
A mixture of 4-chloromethyl-5-methyl-2-phenyloxazole (3.41 g), 3-(4-hydroxyphenyl)propanol (2.50 g), potassium carbonate (3.40 g) and N,N-dimethylformamide (25 ml) was stirred for 14 hours at 60° C. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride, dried (MgSO4), and then concentrated. The residue was subjected to column chromatography on silica gel, and 3-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]propanol (4.46 g, yield 84%) was obtained from a fraction eluted with ethyl acetate-hexane (1:1, v/v) as crystals. Recrystallization from ethyl acetate-hexane gave colorless crystals. m.p. 70-71° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06495581B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-0646657eed2d4dc1b0d400b39be85d20 |
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| Source note | uspto-grants-2002_12 |
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