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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1509656생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1509656

반응식

참여 물질

역할이름HCID투입량
반응물Pivalic acidHCID 6417—
반응물Potassium CarbonateHCID 11430—
반응물7-((2-Bromo-5-chlorophenyl)methoxy)-1,2,3,4-tetrahydronaphthalen-1-oneHCID 69672813—
촉매Tris(4-fluorophenyl)phosphineHCID 140387—
촉매palladium(II) pivalateHCID 24905427—
용매DimethylacetamideHCID 31374—
생성물3-Chloro-10,11-dihydro-5H-benzo(d)naphtho(2,3-b)pyran-8(9H)-oneHCID 6967336667%

반응 조건

온도60 °C

반응 단계

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 dimethylacetamide (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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09221833B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-0cc3e788100b4969ac6ad53794bd3728
출처 메모uspto-grants-2015_12