HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641467Generated: October 27, 2026
Dimethylformamide → 5-chloro-N-(1-cyclopropylethyl)-2-nitrobenzamide
https://huagongshe.com/reaction/1641467
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 5-Chloro-2-nitrobenzoic acid | HCID 17286 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-Cyclopropylethanamine | HCID 519239 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 5-chloro-N-(1-cyclopropylethyl)-2-nitrobenzamide | HCID 43399446 | 75% |
Reaction Steps
A mixed liquid comprising 25 g of 5-chloro-2-nitrobenzic acid, 25 ml of toluene, 22.2 g of thionyl chloride and 0.1 ml of dimethylformamide was refluxed with heating for 1 hour to prepare acid chloride. 18.0 g of triethylamine was added to a mixed solution comprising 13.75 g of 1-cyclopropylethylamine and 375 ml of tetrahydrofuran and cooled with ice. The above prepared acid chloride was dissolved in 30 ml of toluene and dropwise added under cooling with ice. After completion of dropwise addition, reaction was carried out at room temperature for 15 hours. After completion of the reaction, the reaction mixture was poured to water, followed by extraction with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution and dried over sodium sulfate, and ethyl acetate was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 25 g of the pale yellow desired product (melting point: 137 to 141° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08115006B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-44b97b7faad1420f99652d583aba81f3 |
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| Source note | uspto-grants-2012_02 |
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