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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | t-Butyl (2-nitro-3,5,6-trichlorophenyl)acetate | HCID 10688549 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Amino-5,6-dichloro-2-nitrotoluene | HCID 10421042 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05783572 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-512bbff28b704530b97d724f89fb9b6f |
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| Source note | uspto-grants-1998_07 |
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