Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780422Generated: October 31, 2026

Toluene → HCID 53774676, compound

https://huagongshe.com/reaction/1780422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant4-Fluorophenylboronic acidHCID 285645—
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—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 53774676HCID 5377467667%

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), 4-fluorophenylboronic acid (109 mg, 0.78 mmol), 0.65 mL of 2M sodium carbonate solution,1.5 mL of toluene, and 1 mL of methanol, fitted with a reflux condenser, and the stirred mixture was heated at 80°, under nitrogen, for 24 h. The mixture was cooled, diluted with dichloromethane (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 140 mg (67%) of the title compound as a white solid. mp 121°-122°. FDMS: m/e=323. α[D]589 =+79.46 (c=0.99, chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629007
Source datasetuspto-grants-1997_05
ORD IDord-179c781542cc4ed4bb39c68e2a5e9b40
Source noteuspto-grants-1997_05