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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437794Generated: October 30, 2026

Propylene Glycol → HCID 21427097, compound

https://huagongshe.com/reaction/437794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylene GlycolHCID 1030—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantAmmonium HydroxideHCID 14923—
Reactant4-Amino-3-nitrobenzophenoneHCID 596970—
Solvent1-ButanolHCID 263—
SolventTolueneHCID 1140—
ProductHCID 21427097HCID 21427097—

Reaction Steps

A solution of 31.5 parts of (4-amino-3-nitrophenyl)phenylmethanone, 15.2 parts of 1,2-propanediol and 5 parts of 4-methylbenzenesulfonic acid in 40 parts of butanol and 450 parts of methylbenzene is stirred and refluxed for 17 hours. The reaction mixture is cooled and 90 parts of ammonium hydroxide are added (to remove the 4-methylbenzenesulfonic acid). The organic phase is separated, washed with water, dried, filtered and evaporated. The residue is crystallized from methylbenzene. The product is filtered off (the filtrate is set aside), yielding a first fraction of 13.8 parts of 4-(4-methyl-2-phenyl-1,3-dioxolan-2-yl)-2-nitrobenzenamine; mp. 155.2° C. The filtrate, which was set aside, is evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane, methanol and hexane (88:2:10 by volume) as eluent. The pure fractions are collected and the eluent is evaporated, yielding a second fraction of 3.6 parts of 4-(4-methyl-2-phenyl-1,3-dioxolan-2-yl)-2-nitrobenzenamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04032536
Source datasetuspto-grants-1977_06
ORD IDord-6f6518b25fc7476b96d6644b3a747e35
Source noteuspto-grants-1977_06