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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780410Generated: October 31, 2026

Tetrahydrofuran → HCID 54257416, compound

https://huagongshe.com/reaction/1780410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium CarbonateHCID 10340—
Reactant2,3-Dimethylphenylboronic acidHCID 2773395—
Reactant(4aR)-(10bR)-4,10b-dimethyl-8-bromo-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-oneHCID 15355317—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventChloroformHCID 6212—
ProductHCID 54257416HCID 5425741625.4%

Reaction Steps

A 15 mL round bottom flask was charged with (+)-(4aR)-(10bR)-4-methyl-8-bromo-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one (200 mg, 0.65 mmol), tetrakis(triphenylphosphine) palladium (0) (23 mg, 0.02 mmol), 2,3-dimethylphenylboronic acid (117 mg, 0.78 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. The mixture was cooled, diluted with chloroform (50 mL) and washed with brine (2×50 mL). The combined organic extracts were dried over sodium sulfate, concentrated, and purified by silica gel chromatography (ethyl acetate eluent), to give 55 mg (25%) of the title compound as an amorphous solid. mp 133°-140°. FDMS: m/e=333. α[D]589 =+61.90 (c=1.05, methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629007
Source datasetuspto-grants-1997_05
ORD IDord-7cac15855c774a55bb79403328aba422
Source noteuspto-grants-1997_05