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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780489Generated: October 31, 2026

Tetrahydrofuran → HCID 53797615, compound

https://huagongshe.com/reaction/1780489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium CarbonateHCID 10340—
Reactant3-BromoquinolineHCID 21413—
CatalystPalladiumHCID 23938—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventChloroformHCID 6212—
ProductHCID 53797615HCID 5379761556%

Reaction Steps

A 15 mL round bottom flask was charged with (+)-(4aR)-(10bR)-4-methyl-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one-8-boronic acid (178 mg, 0.65 mmol), tetrakis(triphenylphosphine) palladium (0) (23 mg, 0.02 mmol), 3-bromoquinoline (135 mg, 0.65 mmol), 0.65 mL of 2M sodium carbonate solution and 2 mL of THF, fitted with a reflux condenser, and the stirred mixture was heated at 80°, under nitrogen, for 24 h. An additional 23 mg of the palladium reagent was added, and the mixture was heated an additional 24 h. The mixture was cooled, diluted with chloroform (75 mL) and washed with brine (2×25 mL). The combined organic extracts were dried over sodium sulfate, concentrated, and purified by silica gel chromatography (ethyl acetate eluent) to give 130 mg (56%) of the title compound as an amorphous solid. mp: 180°-185°. FDMS: m/e=356. α[D]589 =+80.22 (c=0.37,chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629007
Source datasetuspto-grants-1997_05
ORD IDord-37dd9d93fc9f47ae98912c86476e2852
Source noteuspto-grants-1997_05