HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12211Generated: October 30, 2026
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 67163785, compound
https://huagongshe.com/reaction/12211
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | Oxolane--water (1/1) | HCID 21881883 | — |
| Reactant | HCID 67164779 | HCID 67164779 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67163785 | HCID 67163785 | 75.1% |
Reaction Steps
(6-chloro-1,3,4,9-tetrahydro-β-carbolin-2-yl)-phenyl-methanone (1.76 g, 5.66 mmol, 1 equiv.) and DDQ (2.31 g, 10.2 mmol, 1.8 equiv.) were mixed as solids and cooled to −78° C. 15 ml of a 9:1 THF/H2O solution was cooled to −78° C. and the resulting slurry was added to the cooled solids followed by an additional 15 ml of THF (also cooled to −78° C.). The deep blue solution was stirred at −78° C. for 2 hours and then gradually warmed to room temperature and stirred an additional two hours. The reaction was quenched by the addition of 1 N NaOH, and extracted with 3×150 ml EtOAc. The combined organic layers were washed with 2×100 ml 1 N HCl, 1×100 ml brine, dried over MgSO4, filtered and concentrated to yield 1.38 g (75%) of 2-benzoyl-6-chloro-1,2,3,9-tetrahydro-β-carbolin-4-one as oily orange solids.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07727985B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-a9c8b2ef391f41859897bec5f3ce5352 |
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| Source note | uspto-grants-2010_06 |
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