HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739029Generated: November 3, 2026
Water → Ethyl 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)cinnamate
https://huagongshe.com/reaction/1739029
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzaldehyde | HCID 10708843 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)cinnamate | HCID 53825120 | 81% |
Reaction Steps
Sodium hydride (oily, 60%, 2.40 g) was added little by little to a solution of triethyl phosphonoacetate (12.3 g) in tetrahydrofuran (200 ml) at 0° C., and the mixture was stirred at 10 minutes. Then, 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzaldehyde (14.7 g) was added, and the mixture was stirred at 0° C. for 1 hour. The reaction mixture was poured into water and extracted with ethyl acetate. The ethyl acetate layer was washed with water and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was subjected to column chromatography on silica gel. The fractions eluted with ethyl acetate-hexane (1:3, v/v) gave crystals of ethyl 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)cinnamate (14.8 g, 81%). The crystals were recrystallized from ethanol. Colorless prisms, mp: 94-95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05965589 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-db686117f64945c1a75d56f8696e3a4f |
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| Source note | uspto-grants-1999_10 |
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