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HRID 495900作成日:2026年10月26日

Benzene → 6-Bromo-1,1-dimethyl-4-p-tolyl-1,2-dihydronaphthalene

https://huagongshe.com/reaction/495900

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物1,2,3,4-Tetrahydro-1-hydroxy-1-(4-methylphenyl)-4,4-dimethyl-7-bromonaphthaleneHCID 10545449—
溶媒Diethyl EtherHCID 3283—
生成物6-Bromo-1,1-dimethyl-4-p-tolyl-1,2-dihydronaphthaleneHCID 10687622—

反応手順

A flask equipped with a Dean-Stark trap was charged with 3.4 g of (9.85 mmol) of 1,2,3,4-tetrahydro-1-hydroxy-1-(4-methylphenyl)-4,4-dimethyl-7-bromonaphthalene (Compound C) and 40 ml of benzene. A catalytic amount of p-toluenesulfonic acid monohydrate was added and the resulting solution heated to reflux for 2 hours. Upon cooling to room temperature, Et2O was added and the solution washed with H2O, saturated aqueous NaHCO3, and saturated aqueous NaCl then dried over MgSO4. Removal of the solvents under reduced pressure, and column chromatography (100% hexane/silica gel) afforded the title compound as a colorless solid. 1H NMR (CDCl3): δ 7.32 (1H, dd, J=2.1, 8.2 Hz), 7.21 (5H, m), 7.15 (1H, d, J=2.1 Hz), 5.98 (1H, t, J=4.7 Hz), 2.40 (3H, s), 2.32 (2H, d, J=4.7 Hz), 1.30 (6H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06942980B1
出典データセットuspto-grants-2005_09
ORD IDord-abda2acb42854a239d47af03a4a83cee
出典メモuspto-grants-2005_09