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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532592Generated: October 31, 2026

Hydrochloric Acid → 3,4,5-Trichlorobenzene-1,2-diamine

https://huagongshe.com/reaction/1532592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant2,3,4-Trichloro-6-nitrobenzenamineHCID 10705297—
CatalystIronHCID 23925—
SolventWaterHCID 962—
Product3,4,5-Trichlorobenzene-1,2-diamineHCID 10052972%

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Nitro-2,3,4-trichloroaniline (17.6 g, 72.8 mmol), iron powder (140 g, 250 mmol), and ethanol (400 mL) were combined and the resulting suspension was cooled to 0° C. Concentrated hydrochloric acid (37%, 93 mL, 1.14 mol) was added dropwise over a period of 15 min by means of an addition funnel. When the addition was complete, the resulting suspension was heated to reflux for 3.5 h, after which time it was allowed to cool to room temperature and was subsequently diluted with water (2 L). The pH of the mixture was adjusted to approximately 8 by the slow addition of sodium carbonate. The product was extracted with ethyl acetate (2 L), dried over magnesium sulfate and the solvents were removed under reduced pressure by rotary evaporation. The product was further purified by silica gel chromatography using 65:35 hexane/ethyl acetate to afford 10.9 g (72%) of a tan solid; m.p. 113-115° C. Anal. Calcd for C6H5Cl3N2: C, 34.08; H, 2.38; N, 13.25. Found: C, 34.14; H, 2.41; N, 13.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204249B1
Source datasetuspto-grants-2001_03
ORD IDord-4221687db9134d6793c4bd3f5455e3f6
Source noteuspto-grants-2001_03