Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561913Generated: October 24, 2026

Sodium Hydroxide → 3-Chloro-2,4-dimethylaniline

https://huagongshe.com/en/reaction/561913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantStannous ChlorideHCID 24479—
Reactant2-Chloro-1,3-dimethyl-5-nitrobenzeneHCID 9920569—
Reactant2-Chloro-1,3-dimethyl-4-nitrobenzeneHCID 21396331—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3-Chloro-2,4-dimethylanilineHCID 15278607—

Reaction Steps

To a solution of a mixture 2-chloro-1,3-dimethyl-4-nitro-benzene and chloro-1,3-dimethyl-5-nitro-benzene (12.8 g, 69 mmol) in EtOH (75 mL), conc. HCl (75 mL) was added. Than SnCl2 (51.0 g) was added in two portions. The mixture was stirred overnight at RT, then heated at 60° C. for 30 min, cooled to 0-5° C. (ice bath). Neutralized with NaOH (70 g) in H2O (500 ml). The product was extracted with Et2O (500 ml). Extract was dried over Na2SO4, evaporated. The residue was crystallized two times from hexane providing 3.66 g 3-chloro-2,4-dimethyl-phenylamine as white crystals. The filtrates were evaporated in vacuo and the residue was separated on SiO2 column (200 g), hexane-EtOAc (0 to 10% v/v). providing additionally 3.11 g of the product. Yield 6.77 g (43.5 mmol, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063225B2
Source datasetuspto-grants-2011_11
ORD IDord-dd20f5a271164de1859a54994407fd16
Source noteuspto-grants-2011_11