반응 #2343846
ord-7173ef6c27084fe9b3c52d60234683aa
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후처리
- 1온도The mixture was refluxed for 6 hours under argon atmosphere
- 2여과filtered through celite and
- 3농축concentrated in vacuo
- 4기타Purification by chromatography (silica, 10% EtOAc-hexane)
실험 절차
Employing the above-described procedure for the conversion of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethyl-naphthalene (Compound F) to the dibromonaphthalene derivative (Compound I), 3.5 g (14.6 mmol) of (Compound F), 2.86 g (16.1 mmol) of N-bromosuccinimide and 150 mg (0.62 mmol) of benzoylperoxide gave crude 4,6-dibromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene (Compound I). To a solution of this crude dibromonaphthalene derivative (Compound I) in 50 ml of THF was added 5.38 g (47.1 mmol) of potassium thioacetate. The mixture was refluxed for 6 hours under argon atmosphere, filtered through celite and concentrated in vacuo. Purification by chromatography (silica, 10% EtOAc-hexane) yielded the title compound as red oil.