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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957117Generated: October 26, 2026

Ammonia → 3-Amino-5,6-dichloro-2-nitrotoluene

https://huagongshe.com/reaction/1957117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactantt-Butyl (2-nitro-3,5,6-trichlorophenyl)acetateHCID 10688549—
SolventWaterHCID 962—
Solvent2-MethoxyethanolHCID 8019—
SolventEthyl AcetateHCID 8857—
Product3-Amino-5,6-dichloro-2-nitrotolueneHCID 10421042—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of t-butyl (2-nitro-3,5,6-trichlorophenyl)acetate (123 g, 0.361 mol) and saturated aqueous ammonia (300 mL) in 2-methoxy ethanol (360 mL) was heated in an autoclave at 150° C. for 72 hours. The resulting viscous, black mixture was diluted with water (1 L) and ethyl acetate (1 L) and filtered through Arbocel filter aid. The dark red filtrate was separated, and the aqueous layer extracted with ethyl acetate (2×1 L). The combined organic solutions were washed with brine (1 L), dried (MgSO4) and evaporated onto silica gel (70-200μ, 200 g). The silica gel was applied to the top of a chromatography column containing silica gel (40-60 μ, 800 g). Elution with hexane/ethyl acetate (98:2-92:8) gave 3-amino-5,6-dichloro-2-nitrotoluene (EP-A-0385850) as a bright orange solid (39.7 g), which was contaminated with 5-amino-3,6-dichloro-2-nitrotoluene (14%). This mixture was carried onto the next step without further purification. 1H NMR (300 MD, CDCl3) 2.48 (3H, s), 4.80 (2H, s), 6.82 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783572
Source datasetuspto-grants-1998_07
ORD IDord-512bbff28b704530b97d724f89fb9b6f
Source noteuspto-grants-1998_07