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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284925Generated: November 1, 2026

Ethylene Glycol → HCID 70456308, compound

https://huagongshe.com/reaction/1284925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant1,1-DichloroethaneHCID 6365—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 13491592HCID 13491592—
SolventWaterHCID 962—
ProductHCID 70456308HCID 70456308—

Reaction Steps

100 ml of dichloroethane are added to 20.6 g (0.0624 mol) of 8-methyl-6-phenyl-6,7,8,9-tetrahydro-1H-pyrido[4,3-g]indole-2,3-dione, 21 ml (0.374 mol) of ethylene glycol and 0.336 g (0.00176 mol) of toluene-4-sulphonic acid monohydrate, with stirring, and the mixture is heated under reflux for 3.5 hours, using a water separator. Ice is added to the reaction mixture and the mixture is brought to pH 6.8 with aqueous KHCO3 solution. The mixture is extracted with CH2Cl2, the CH2Cl2 phase is washed with H2O and dried over Na2SO4 and the solvent is stripped off in a rotary evaporator. The residue is chromatographed on Al2O3 (aluminum oxide from E. Merck, Darmstadt) using an eluent mixture of ethyl acetate and MeOH (20:0.2). After trituration with ethyl acetate/petroleum ether, the substance becomes crystalline. It is dried over P2O5 at 80° C. in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04564613
Source datasetuspto-grants-1986_01
ORD IDord-38865ff46e164f72a92c0d16454caa7f
Source noteuspto-grants-1986_01