HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079185Generated: October 31, 2026
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 54544880, compound
https://huagongshe.com/reaction/1079185
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | HCID 21649150 | HCID 21649150 | — |
| Reactant | HCID 54527235 | HCID 54527235 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 54544880 | HCID 54544880 | 20.4% |
Reaction Steps
To a suspension of (+)-(4aR)-(10bR)-8-(1-naphthyl)-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]-quinolin-3-one (295 mg, 0.865 mmol), in 3.5 mL of 1,4-dioxane was added DDQ (216 mg, 1.1 equiv.) followed by bistrimethylsilyltrifluoromethyl acetamide (998 mg, 4.5 equiv.), and the solution was stirred at room temperature for 2 h, then heated at 100° for 20h. The mixture was cooled to room temperature, diluted with ethyl acetate, and washed with 2M sodium hydroxide. The organic phase was washed with brine, dried over sodium sulfate, concentrated and chromatographed on silica gel (ethyl acetate eluent) to give, after trituration from ether/hexanes, 60 mg (20%) of the title compound as a white solid. mp 199°-201° (decomp.) FDMS m/e=339. α[D]589 =+35.98 (c=0.67, 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-cfa12c2ff49d494c9517a2a3ba60d52a |
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| Source note | uspto-grants-1996_08 |
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