HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106239Generated: October 31, 2026
Morpholine → (3,4-Dinitrophenyl)(morpholino)methanone
https://huagongshe.com/reaction/1106239
Participants
| Role | Name | HCID | Charge |
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| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 3,4-dinitrobenzoyl Chloride | HCID 11806491 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3,4-Dinitrophenyl)(morpholino)methanone | HCID 13043973 | — |
Reaction Steps
A solution of 17.4 g (0.075 mol.) of 3,4 dinitrobenzoylchloride in 250 ml of methylene chloride is treated at 0°-20° C. with a solution of 13 g. (0.15 mol.) of morpholine in 100 ml. of methylene chloride. The solution is kept at 20°-25° C. for 2 hrs., the solvent is evaporated and the residue triturated with water. Recrystallization from methanol affords 4-morpholinocarbonyl-1,2-dinitrobenzene (m.p. 136°-137° C.). 17.0 G. of 4-morpholinocarbonyl-1,2-dinitrobenzene in 340 ml. of methanol is hydrogenated for 3 hrs. at 45-50 psi in the presence of 1.7 g. of 5% palladized charcoal. The resulting solution of 1,2-diamino-4-morpholinocarbonylbenzene is filtered and concentrated to ~170 ml. 14.0 G. of 1,3-bis-methoxycarbonyl-S-methyl isothiourea, 170 ml. of water and 4 ml. of acetic acid are added to the diamine solution and the mixture is refluxed for 3 hrs. The solution is concentrated and cooled. Filtration and recrystallization from methanol-chloroform affords 5(6)-morpholinocarbonyl-2-carbomethoxyaminobenzimidazole (m.p. 224° C. dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04312873 |
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| Source dataset | uspto-grants-1982_01 |
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| ORD ID | ord-ce5a11e07eb14684a777c4995dca4b60 |
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| Source note | uspto-grants-1982_01 |
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