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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374545Generated: October 30, 2026

Water → HCID 14116044, compound

https://huagongshe.com/reaction/374545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantHCID 14116041HCID 14116041—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
ProductHCID 14116044HCID 1411604476.4%

Reaction Steps

The hydrocarbon (5) 48 mg; 0.22 mmol) was dissolved in hot acetic acid (15 ml) and water (5 ml) was added slowly with stirring to maintain homogeneity of the solution. 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) (198 mg, 0.88 mmol) was added, changing the color of the solution to dark green. Stirring was continued at reflux for 30 min. during which time the color of the solution changed to dark red. The reaction mixture was cooled and diluted with ether, and the ether layer was washed with water and aqueous NaOH. The solution was dried over MgSO4 and evaporated to provide a white solid which was chromatographed on a column of Florisil™. Elution with ether yielded 6 (39 mg, 76%):m.p. 127°-128° C.; NMR δ272 (t,1,H15 or 16), 2.85-2.91 (m,4,H6,7), 3.07 (t,1,H15 or 16), 7.24-7.31 (m,3,H2,3,4), 7.67-7.77 (m,3,H1,11,12). Anal. Calc'd. for C17H14O: C,87.25; H,6.02. Found: C,87.13; H,6.03.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05480913
Source datasetuspto-grants-1996_01
ORD IDord-d69da1715ef84b578fead0f2b3b94e35
Source noteuspto-grants-1996_01