HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093620Generated: October 31, 2026
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 68725848, compound
https://huagongshe.com/reaction/2093620
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | HCID 57917216 | HCID 57917216 | — |
| Reactant | HCID 77231520 | HCID 77231520 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68725848 | HCID 68725848 | 35.8% |
Reaction Steps
Methyl-2-formylpyrimidine-5-carboxylate (200 mg, 1.205 mmol) and 3-amino-4-hydroxy-5-isopropylbenzonitrile (212 mg, 1.205 mmol) were dissolved in methanol (5 ml). The mixture was concentrated, and then the residue was dissolved in dichloromethane (5 ml). To the above solution was added 2,3-dichloro-5,6-dicyano-p-benzoquinone (300.9 mg, 1.325 mmol) at room temperature. The solution was stirred at room temperature for 30 min, and then concentrated. The residue was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The aqueous layer was extracted with ethyl acetate (3×). The combined organics were washed with brine, dried over magnesium sulfate, and concentrated. The residue was purified by flash chromatography (hexanes-ethyl acetate=4:1, then 1:1) to provide of the title compound (139 mg) as a yellow solid. Mass spectrum (ESI) 322.8 (M+1). 1H NMR (500 MHz, CDCl3) δ 9.55 (s, 2H), 8.13 (s, 1H), 7.66 (s, 1H), 4.09 (s, 3H), 3.65 (m, 1H), 1.50 (d, 6H, J=6.8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445480B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-91034a59220d4b45a7b366d8c1e8f212 |
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| Source note | uspto-grants-2013_05 |
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