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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518890Generated: November 2, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 10583334, compound

https://huagongshe.com/reaction/1518890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantSodium ThiosulfateHCID 24477—
ReactantHCID 68265910HCID 68265910—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 10583334HCID 10583334—

Reaction Steps

To an aqueous solution of 10-((4-methoxybenzyl)oxy)-1-decene-3-ol (590 mg, 2.02 mmol, 1.00 eq.) in methylene chloride (20.0 mL) and saturated sodium bicarbonate (10.0 mL), was added DDQ (687 mg, 3.03 mmol, 1.50 eq.) at room temperature. The mixture was allowed to react at the same temperature for 5 hours, and then the reaction solution was poured into 10% aqueous sodium thiosulfate solution. The organic phase was extracted with ethyl acetate, and then the resulting organic phase was washed with 10% aqueous sodium thiosulfate solution, a saturated aqueous sodium bicarbonate solution, and a saturated salt solution. The washed organic phase was dried over magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=70:30) to obtain 1-decene-3,10-diol as shown below (324 mg, 1.88 mmol, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073802B2
Source datasetuspto-grants-2015_07
ORD IDord-3170f7e36fbb41679f8c605ad5274e83
Source noteuspto-grants-2015_07