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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079154Generated: October 31, 2026

Tetrahydrofuran → HCID 54188410, compound

https://huagongshe.com/reaction/1079154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium CarbonateHCID 10340—
Reactant(Naphthalen-2-yl)boronic acidHCID 2734375—
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 54188410HCID 5418841055%

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-naphthylboronic acid (168 mg, 0.98 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° for 16 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 126 mg (55%) of the title compound as a white solid. mp 221°-223°. FDMS: m/e=355. α[D]589 =+73.58 (c=1.06, chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550134
Source datasetuspto-grants-1996_08
ORD IDord-a5768a5c93ee417ea502eaaf0d2a5218
Source noteuspto-grants-1996_08