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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantHCID 21649150HCID 21649150—
ReactantHCID 54527235HCID 54527235—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 54544880HCID 5454488020.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550134
Source datasetuspto-grants-1996_08
ORD IDord-cfa12c2ff49d494c9517a2a3ba60d52a
Source noteuspto-grants-1996_08