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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684109Generated: November 3, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 135500131, compound

https://huagongshe.com/reaction/1684109

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantPotassium BromideHCID 253877—
ReactantButanol acetic acid waterHCID 22056973—
ReactantHCID 135404972HCID 135404972—
SolventMethanolHCID 887—
ProductHCID 135500131HCID 135500131—

Reaction Steps

To 105 mg (0.244 mmol) of 18 suspended in 15 mL of dry methanol, was added 61 mg (0.268 mmol) of dichlorodicyanobenzoquinone (DDQ) and the reaction left to stir at room temperature for 1 hour. The solids were filtered off, washed with methanol, and dried to afford pure 19: 95 mg (91%) yield; dec pt 274°-275° C.; TLC (n-butanol/acetic acid/water [5:2:3]), Rf =0.46; IR (KBr pellet) 3062, 3040, 2990, 2933, 1713, 1645, 1576, 1547, 1480, 1142 cm-1 ; 1H NMR (dimethyl-d6 sulfoxide) δ4.45 (4H, s, methylenes); mass spectrum (EI, solids probe), m/z 428, 430, and 432 (P+ for the 79Br, 79Br; 79Br, 81Br, 81Br, 81Br combinations, respectively, in an intensity ratio of 1:2:1). Anal. Calcd for C12H6Br2N4O4 ; C, 33.52; H, 1.41; N, 13.03. Found: C, 33.89; H, 1.31; N, 12.50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639881
Source datasetuspto-grants-1997_06
ORD IDord-e782cd09779a465a8bb0a9a91a053d03
Source noteuspto-grants-1997_06