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HRID 1751598作成日:2026年10月25日

Pivalic acid → 3-Chloro-10,11-dihydro-5H-benzo(d)naphtho(2,3-b)pyran-8(9H)-one

https://huagongshe.com/reaction/1751598

反応式

関与物質

役割名称HCID仕込み量
反応物Pivalic acidHCID 6417—
反応物Potassium CarbonateHCID 11430—
反応物7-((2-Bromo-5-chlorophenyl)methoxy)-1,2,3,4-tetrahydronaphthalen-1-oneHCID 69672813—
触媒Tris(4-fluorophenyl)phosphineHCID 140387—
触媒palladium(II) pivalateHCID 24905427—
溶媒DimethylacetamideHCID 31374—
生成物3-Chloro-10,11-dihydro-5H-benzo(d)naphtho(2,3-b)pyran-8(9H)-oneHCID 6967336667%

反応条件

温度60 °C

反応手順

To a 1 L flask containing palladium(II) pivalate (1.18 g, 3.8 mmol), tri(4-fluorophenyl)phosphine (1.20 g, 3.8 mmol), pivalic acid (2.33 g, 22.8 mmol) and potassium carbonate (31.8 g, 228 mmol) was added a solution of 7-(2-bromo-5-chlorobenzyloxy)-3,4-dihydronaphthalen-1(2H)-one (27.8 g, 76.2 mmol) in dimethyacetamide (380 mL). The flask was evacuated and backfilled with argon 5 times and then stirred under argon at 60° C. for 24 hours. The reaction was cooled to room temperature and diluted with MTBE and water. The resulting biphasic mixture was stirred for 3 hours and filtered through Celite, rinsing with MTBE. The organic layer of the filtrate was separated and then washed twice with water and once with brine. The organics were then dried with magnesium sulfate, filtered, concentrated and purified by flash column chromatography (Hexanes/DCM) to yield 3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (14.4 g, 67% yield) as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09156823B2
出典データセットuspto-grants-2015_10
ORD IDord-242b6563ca374907a2460cccf4ef29ea
出典メモuspto-grants-2015_10