HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639629Generated: October 28, 2026
Morpholine → (3,4-Dinitrophenyl)(morpholino)methanone
https://huagongshe.com/reaction/1639629
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,4-Dinitrobenzoic acid | HCID 10709 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3,4-Dinitrophenyl)(morpholino)methanone | HCID 13043973 | 96.1% |
Reaction Steps
A solution of 3,4-dinitrobenzoic acid (10 g, 47 mmol, 1 eq.) and DMF (0.1 mL) in THF (100 mL) was treated with thionyl chloride (4.5 mL, 62 mmol, 1.3 eq.) then heated to reflux for 2.5 h. The mixture was cooled in ice then triethylamine (10 mL, 71 mmol, 1.1 eq.) was added over 20 min, keeping internal temperature<5° C. Morpholine (6.2 mL, 71 mmol, 1.5 eq) was added to the resulting thick yellow suspension over 15 min, keeping internal temperature<10° C. The ice-bath was removed and the mixture allowed to warm to r.t. After 15 min, a further portion of morpholine (1 mL, 11 mmol, 0.24 eq.) was added and the mixture stirred overnight. The mixture was diluted with water (250 mL) and cooled in ice. A beige solid was filtered off under suction, washed with a further portion of cold water (25 mL) and dried in vacuo to afford the title compound (12.7 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110573B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-880b650c2bdd44bb9475f5111fd93103 |
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| Source note | uspto-grants-2012_02 |
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