HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079151Generated: October 25, 2026
Dimethyl Ether → (+)-(4aR)-(10bR)-4-methyl-8-(9-phenanthrenyl)-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one
https://huagongshe.com/reaction/1079151
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Ether | HCID 8254 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 9-Phenanthracenylboronic acid | HCID 11775704 | — |
| Reactant | (4aR)-(10bR)-4,10b-dimethyl-8-bromo-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one | HCID 15355317 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (+)-(4aR)-(10bR)-4-methyl-8-(9-phenanthrenyl)-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one | HCID 53706214 | 30.3% |
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), 9-phenanthreneboronic acid (173 mg, 0.78 mmol), triethylamine (0.2 mL, 1.3 mmol), and 2 mL of dimethyl ether, 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 (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 80 mg (30%) of the title compound as a white solid. mp 218°-220°. FDMS: m/e=405. α[D]589 =+63.01 (c=0.98, chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05550134 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-334ab6f888bd4a5095ae31afdc9edff4 |
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| Source note | uspto-grants-1996_08 |
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