HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925389Generated: October 28, 2026
Benzoyl chloride, 3-nitro- → HCID 883681, compound
https://huagongshe.com/reaction/1925389
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl chloride, 3-nitro- | HCID 8495 | — |
| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 883681 | HCID 883681 | 107% |
Reaction Steps
3-Nitrobenzoyl chloride (2 g, 10.77 mmol) was loaded into a round bottomed flask, placed under a N2 atmosphere and dissolved in anhydrous DCM (10 mL). The mixture was cooled to 0° C. and N,N-dimethylethylenediamine (0.98 mL, 8.98 mmol) was added to the reaction. The reaction was allowed to warm to RT and left to stir for 18 h. After 18 h the reaction had given a precipitate which was isolated by filtration and washed with DCM to give 2.28 g of a white solid, which was partitioned between DCM and a saturated aqueous NaHCO3 solution. The organic layer was removed under reduced pressure and the aqueous layer was then re-extracted DCM. The organic layers were combined, dried over Na2SO4 and the solvent was removed under reduced pressure to afford the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178557B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-b2c4438211a348d3840b213f71bff298 |
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| Source note | uspto-grants-2012_05 |
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