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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
Reactant2-[2-[(3-Methoxyphenyl)methyl]cyclohexyl]-4,5-diphenyloxazoleHCID 19358416—
SolventDichloromethaneHCID 6344—
Product2-[2-[(3-Hydroxyphenyl)methyl]-cyclohexyl]-4,5-diphenyloxazoleHCID 1935849684.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06025375
Source datasetuspto-grants-2000_02
ORD IDord-8a59e5ba56ce47769dbd4913b64b8dab
Source noteuspto-grants-2000_02