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HRID 1215作成日:2026年10月25日

Cyclohexanol → 6-Bromo-4-cyclohexyloxy-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/1215

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexanolHCID 7966—
反応物SodiumHCID 5360545—
反応物4,6-Dibromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthaleneHCID 19694961—
生成物6-Bromo-4-cyclohexyloxy-1,1-dimethyl-1,2,3,4-tetrahydronaphthaleneHCID 19694963—

反応条件

温度70 °C

反応手順

To 9 g (89.9 mmol) of cyclohexanol was added 160 mg (7.0 mmol) of sodium metal and the mixture was stirred at 70° C. for 12 hours. After all of the sodium dissolved the reaction mixture was cooled to ambient temperature and then a solution of 1 g (3.2 mmol) of 4,6-dibromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene (Compound I) in 1 ml of cyclohexanol was added. The mixture was heated at 120° C. for 4 hours and thereafter the excess solvent distilled off under reduced pressure. The product was dissolved in Et2O (75 ml), washed with water (5 ml) and brine (5 ml), dried over MgSO4 and concentrated in vacuo. Purification by column chromatography (silica, 5% EtOAc-hexane) yielded the title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723620
出典データセットuspto-grants-1998_03
ORD IDord-d9d51c679b094d58b2ae53013e4113f3
出典メモuspto-grants-1998_03