HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187478Generated: October 26, 2026
Triethylamine → Diisopropylether ethyl acetate
https://huagongshe.com/reaction/2187478
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(Morpholine-4-carbonyl)aniline | HCID 577815 | — |
| Reactant | 5-Methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid | HCID 18622509 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-Morpholinocarbonylphenyl)-5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxamide | HCID 18622500 | — |
| Product | Diisopropylether ethyl acetate | HCID 22281796 | 315.3% |
Reaction Steps
A mixture of 5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (1.0 g, 4 mmol), toluene (20 mL), N,N-dimethylformamide (10 drops) and thionyl chloride (1.5 mL, 20 mmol) was heated at 60° C. for 1 h. The solvents were removed in vacuo and the residue, dissolved in methylene chloride (20 mL), was added to a solution of 4-aminobenzoylmorpholine (820 mg, 4 mmol, described in: Devlin J.P. J. Chem. Soc. Perkin Trans I, 1975, 830-841) and triethylamine (800 mg, 8 mmol) in methylene chloride (30 mL) at 5° C. After stirring at 20° C. for 2 h, water was added and the organic phase was separated, dried and the solvent removed in vacuo. The oily residue was crystallized from diisopropyl ether/ethyl acetate affording 1.2 g (73% yield) of the title compound as crystals: mp 186-189° C.; EIMS (70 eV) m/z (relative intensity) 439 (20, M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06410532B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-dc87a79c201c47a690d0746e989a239e |
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| Source note | uspto-grants-2002_06 |
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