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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249511Generated: October 26, 2026

Ethylene Glycol → 1-(3,4-Dimethoxyphenyl)-5,5-ethylenedioxy-7-(4-methoxyphenyl)-2-nitroheptane

https://huagongshe.com/reaction/1249511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantBenzeneHCID 241—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1-(3,4-Dimethoxyphenyl)-7-(4-methoxyphenyl)-2-nitro-5-heptanoneHCID 13065020—
SolventWaterHCID 962—
Product1-(3,4-Dimethoxyphenyl)-5,5-ethylenedioxy-7-(4-methoxyphenyl)-2-nitroheptaneHCID 13065021—

Reaction Steps

Into a 1 l. r.b. flask equipped with a Dean-Stark trap was placed 22 g. (0.055 mole) of 1-(3,4-dimethoxyphenyl)-7-(4-methoxyphenyl)-2-nitro-5-heptanone, 2 g. of p-toluenesulfonic acid, 25 ml. of ethylene glycol, and 500 ml. of benzene, the mixture was refluxed until no more water was separated, and then cooled to room temperature. The dark solution was poured into cold dil. NaHCO3 solution and extracted with ethyl acetate. The organic layer was backwashed with water and dried over anhydrous MgSO4. Upon removing solvent by distillation a gray solid was obtained from trituration with ether. Recrystallization from 80% ethanol yielded 25 g. of product as a white solid; m.p. 98°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04632929
Source datasetuspto-grants-1986_12
ORD IDord-b6e2c501f48f477f8e38ba70edceecf2
Source noteuspto-grants-1986_12