HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377300Generated: October 30, 2026
Ethyl Acetate → 2-[2-[(3-Hydroxyphenyl)methyl]-cyclohexyl]-4,5-diphenyloxazole
https://huagongshe.com/reaction/377300
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-[2-[(3-Methoxyphenyl)methyl]cyclohexyl]-4,5-diphenyloxazole | HCID 19358416 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[2-[(3-Hydroxyphenyl)methyl]-cyclohexyl]-4,5-diphenyloxazole | HCID 19358496 | 84.7% |
Reaction Steps
1.0 M Solution of boron tribromide in dichloromethane (1.25 ml) was added dropwise to a stirred solution of 2-[2-[(3-methoxyphenyl)methyl]cyclohexyl]-4,5-diphenyloxazole (370 mg) in dichloromethane (2.0 ml) under ice cooling. The resulting mixture was stirred at the same temperature for 2 hours and at room temperature for 22 hours, and then a mixture of ethyl acetate and sodium bicarbonate aqueous solution was added thereto. The organic layer was washed with sodium bicarbonate aqueous solution and brine, dried over magnesium sulfate, and evaporated in vacuo. The oily residue was chromatographed over silica gel using n-hexane--ethyl acetate as an eluent to afford 2-[2-[(3-hydroxyphenyl)methyl]-cyclohexyl]-4,5-diphenyloxazole (303 mg) as a syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06025375 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-8a59e5ba56ce47769dbd4913b64b8dab |
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| Source note | uspto-grants-2000_02 |
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