HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437794Generated: October 30, 2026
Propylene Glycol → HCID 21427097, compound
https://huagongshe.com/reaction/437794
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propylene Glycol | HCID 1030 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 4-Amino-3-nitrobenzophenone | HCID 596970 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21427097 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04032536 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-6f6518b25fc7476b96d6644b3a747e35 |
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| Source note | uspto-grants-1977_06 |
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