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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58146Generated: October 25, 2026

Dimethylamine → 4-[(Dimethylamino)methyl]-2-nitroaniline

https://huagongshe.com/reaction/58146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Amino-3-nitrobenzaldehydeHCID 13237703—
CatalystHCID 178460666HCID 178460666—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product4-[(Dimethylamino)methyl]-2-nitroanilineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434697B2
Source datasetuspto-grants-2016_09
ORD IDord-f9d6f6fc983a4f7f931e3fb810215a6f
Source noteuspto-grants-2016_09