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HRID 1214作成日:2026年10月26日

Benzoyl Peroxide → 4,6-Dibromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/1214

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl PeroxideHCID 7187—
反応物N-bromobutanimideHCID 67184—
反応物6-Bromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthaleneHCID 10586063—
溶媒Carbon TetrachlorideHCID 5943—
生成物4,6-Dibromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthaleneHCID 19694961—

反応手順

To a solution of 1.2 g (5.0 mmol) of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene (Compound F) in 20 ml of CCl4 was added 0.97 g (5.5 mmol) of N-bromosuccinimide followed by 20 mg (0.08 mmol ) of benzoylperoxide. The mixture was refluxed for 3 hours, filtered and the filtrate washed with water (5 ml). The organic phase was dried over MgSO4 and then concentrated in vacuo to yield the title compound as a pale yellow 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-d35af9b12f1b47e88a643494fdc123b8
出典メモuspto-grants-1998_03