HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58146Generated: October 25, 2026
Dimethylamine → 4-[(Dimethylamino)methyl]-2-nitroaniline
https://huagongshe.com/reaction/58146
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Amino-3-nitrobenzaldehyde | HCID 13237703 | — |
| Catalyst | HCID 178460666 | HCID 178460666 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[(Dimethylamino)methyl]-2-nitroaniline | HCID 62183213 | — |
Reaction Steps
To a stirred solution of dimethylamine (4.0 mL, 2 M, 8.0 mmol) in MeOH (4 mL) was added Ti(OiPr)4 (1.15 g, 4 mmol) and the solution was stirred at room temperature for 15 minutes Then 4-amino-3-nitro-benzaldehyde (160 g, 1.0 mmol) in MeOH (2 mL) was added and the solution was stirred at room temperature overnight. Then NaBH4 (78 g, 2 mmol) was added and the solution was stirred at room temperature for 1 hour. LCMS showed major product peak. The solution was diluted with EtOAc (60 mL) and washed with water (2×100 mL) and brine (50 mL), dried over anhydrous Na2SO4. The solution was evaporated to dryness and 130 mg of crude product was collected, which was used for the next step without further purification, 1H NMR (400 MHz, DMSO-d6) δ 7.82 (s, 1H), 7.35 (br s, 2H), 7.31 (dd, 1H), 6.97 (d, 1H), 3.26 (s, 2H), 2.12 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434697B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-f9d6f6fc983a4f7f931e3fb810215a6f |
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| Source note | uspto-grants-2016_09 |
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