HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12620Generated: October 30, 2026
Dimethylamine → N,N-dimethyl-1-(2-methyl-4-nitro-1H-indol-3-yl)methanamine
https://huagongshe.com/reaction/12620
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1H-Indole, 2-methyl-4-nitro- | HCID 11095150 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N,N-dimethyl-1-(2-methyl-4-nitro-1H-indol-3-yl)methanamine | HCID 68689213 | — |
Reaction Steps
To an acetic acid (5 mL) solution of an aqueous 370% formaldehyde solution (271 mg), an aqueous 50% dimethylamine solution (317 mg) was slowly added dropwise under ice cooling and the mixture was stirred at room temperature for 30 minutes. Furthermore, an acetic acid (1 mL) solution of 2-methyl-4-nitro-1H-indole [Tetrahedron 1, 1999, 5395-5398] (310 mg) was added and the mixture was stirred at room temperature for 24 hours. The pH of the reaction mix was adjusted to 9 using an aqueous 5M sodium hydroxide solution, followed by extraction with dichloromethane three times. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate and then concentrated. The residue was washed with diisopropyl ether to obtain the titled compound having the following physical properties (303 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07728023B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-3e013e4fe1c942929986588c683791e1 |
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| Source note | uspto-grants-2010_06 |
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