HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968934Generated: November 1, 2026
2-Methyl-5-Nitroaniline → HCID 67494403, compound
https://huagongshe.com/reaction/1968934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methyl-5-Nitroaniline | HCID 7444 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 77139281 | HCID 77139281 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67494403 | HCID 67494403 | — |
Reaction Steps
To a suspension of the product of step 3 (2.05 g) in anhydrous dichloromethane (30 ml), a solution of 2-methyl-5-nitroaniline (3.04 g) and triethylamine (8 ml, excess allowed) in dichloromethane (15 ml) was added dropwise slowly in an ice-bath with the temperature no more than 5° C. After addition, the reaction was carried out for 30 min in an ice-bath, and then at room to temperature for 3 h. Completion of reaction was indicated by TLC. Potassium carbonate solution (10%) was added to the mixture. Then the mixture was extracted with EtOAc (20 ml*3). The organic layer was dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure to recover the solvent. The residue was purified on silica gel column (EtOAc/petroleum ether 4:1). The eluent was collected, concentrated under reduced pressure to give a yellow powdered solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426446B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-125f4960c91b435b966dc736ef854f8b |
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| Source note | uspto-grants-2013_04 |
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