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HRID 514110作成日:2026年10月26日

7-Bromo-3-methylnaphthalen-1-ol → 1-Naphthol, 3-methyl-

https://huagongshe.com/reaction/514110

反応式

関与物質

役割名称HCID仕込み量
反応物7-Bromo-3-methylnaphthalen-1-olHCID 67126282—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物1-Naphthol, 3-methyl-HCID 26135—

反応条件

温度23 °C

反応手順

A slurry of 7-bromo-3-methylnaphthalen-1-ol (100 mg, 0.421 mmol), 10% w/w Pd/C (45 mg, 42.1 μmol Pd), and absolute EtOH (2.0 mL) was purged under vacuum and backfilled with H2 from a balloon several times. The suspension was stirred under a balloon of H2 at 23° C. overnight. The reaction was filtered over Celite, the cake was washed with EtOAc. The filtrate was concentrated and dissolved in DCM. The solution was wet-loaded onto a 12 g “gold” ISCO silica gel column and purified by flash chromatography (ethyl acetate/hexanes) giving the desired product (yield was not found). 1H NMR (400 MHz, CDCl3) δ 8.10 (d, J=7.8 Hz, 1H), 7.72 (d, J=7.8 Hz, 1H), 7.47-7.39 (m, 2H), 7.22 (s, 1H), 6.67 (s, 1H), 2.45 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09102614B2
出典データセットuspto-grants-2015_08
ORD IDord-76f4a0cb7efe4d6ebbadd81f5cd2e57d
出典メモuspto-grants-2015_08