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HRID 1509656Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1509656

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPivalic acidHCID 6417—
EduktPotassium CarbonateHCID 11430—
Edukt7-((2-Bromo-5-chlorophenyl)methoxy)-1,2,3,4-tetrahydronaphthalen-1-oneHCID 69672813—
KatalysatorTris(4-fluorophenyl)phosphineHCID 140387—
Katalysatorpalladium(II) pivalateHCID 24905427—
LösungsmittelDimethylacetamideHCID 31374—
Produkt3-Chloro-10,11-dihydro-5H-benzo(d)naphtho(2,3-b)pyran-8(9H)-oneHCID 6967336667%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09221833B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-0cc3e788100b4969ac6ad53794bd3728
Quellennotizuspto-grants-2015_12