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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379474Generated: October 30, 2026

Toluene → HCID 54197412, compound

https://huagongshe.com/reaction/1379474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
ReactantN-Dansyl-3-aminobenzeneboronic acidHCID 150643—
Reactant(4aR)-(10bR)-4,10b-dimethyl-8-bromo-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-oneHCID 15355317—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 54197412HCID 5419741263%

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 (83 mg, 0.27 mmol), tetrakis (triphenylphosphine)palladium(0) (23 mg, 0.02 mmol), 3-dansylaminophenylboronic acid (99 mg, 0.27 mmol), 0.3 mL of 2M sodium carbonate solution, 0.5 mL of toluene, and 0.1 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 94 mg (63%) of the title compound as a yellow solid. mp 130°-140° (decomp.) FDMS: m/e=553. α[D]589 =+3.01 (c=1.03 methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670514
Source datasetuspto-grants-1997_09
ORD IDord-ecd556aa058543e78eda7e7017f4715e
Source noteuspto-grants-1997_09