Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079153Generated: October 31, 2026

Tetrahydrofuran → HCID 54032512, compound

https://huagongshe.com/reaction/1079153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium CarbonateHCID 10340—
Reactant(2H-1,3-benzodioxol-5-yl)boronic acidHCID 2734371—
Reactant4-Methyl-8-bromo-10b-methyl-1,2,3,4,4a, 5,6,10b-octahydrobenzo[f]quinolin-3-oneHCID 22125219—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventChloroformHCID 6212—
ProductHCID 54032512HCID 5403251257.2%

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), 3,4-methylenedioxyphenyl boronic acid (131 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 (2×25 mL). The combined organic extracts were dried over sodium sulfate, concentrated, and purified by silica gel chromatography (ethyl acetate eluent), to give 130 mg (57%) of the title compound as an amorphous solid. mp 146°-152° FDMS: m/e=349. α[D]589 =+67.92 (c=1.06, chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550134
Source datasetuspto-grants-1996_08
ORD IDord-d5db75131e8d4dbebd1eb0f4ca8eced4
Source noteuspto-grants-1996_08