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HRID 1049622作成日:2026年10月26日

Triphenylphosphine → 3,4-dihydro-6-methylnaphthalen-1(2H)-one

https://huagongshe.com/reaction/1049622

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Methylboronic AcidHCID 139377—
反応物6-Bromo-1-tetraloneHCID 10105069—
触媒palladium(II) acetateHCID 167845—
溶媒TetrahydrofuranHCID 8028—
生成物3,4-dihydro-6-methylnaphthalen-1(2H)-oneHCID 16262088%

反応手順

A solution of 19 (1.4 g, 6.1 mmol), methyl boronic acid (0.6 g, 9.3 mmol), Pd(OAc)2 (0.07 g, 0.31 mmol), PPh3 (0.16 g, 0.61 mmol), and K3PO4 (5.2 g, 24 mmol) in dry THF were stirred at reflux under N2 atm overnight. After cooling at room temperature, crude was filtered through celite, concentrated by rotary evaporation, and purified by column chromatography to give 6-methyl-3,4-dihydronaphthalen-1(2H)-one (20) (88%). 1H NMR (600 MHz, CDCl3) δ 7.93 (d, J=12.0 Hz, 1H), 7.11 (d, J=12.0 Hz, 1H), 7.06 (s, 1H), 2.92 (t, J=6.0 Hz, 2H), 2.63 (t, J=12.0 Hz, 2H), 2.37 (s, 3H), 2.13-2.10 (m, 2H). GC-MS (ES) for C11H12O [M]+ 160.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09382245B2
出典データセットuspto-grants-2016_07
ORD IDord-d605d5ded35a41ffab5dceefbd1d25c7
出典メモuspto-grants-2016_07