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HRID 1751598Erstellt: 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/1751598

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 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09156823B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-242b6563ca374907a2460cccf4ef29ea
Quellennotizuspto-grants-2015_10