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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535720Generated: October 30, 2026

Hydrochloric Acid → 3-Bromo-5-chloro-2-fluorobenzenamine

https://huagongshe.com/reaction/535720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCarbamic acid, N-(3-bromo-5-chloro-2-fluorophenyl)-, 1,1-dimethylethyl esterHCID 51034463—
Solvent1,4-DioxaneHCID 31275—
Product3-Bromo-5-chloro-2-fluorobenzenamineHCID 51034225—

Reaction Steps

tert-Butyl 3-bromo-5-chloro-2-fluorophenylcarbamate (1.0 g, 3.1 mmol) was treated with 4.0 M HCl in dioxane (10 mL) and the resulting reaction was maintained at room temperature for 4 hours. The reaction mixture was concentrated and partitioned between EtOAc (200 mL) and saturated aqueous NaHCO3 solution (75 mL). The layers were separated and the organic portion was washed with brine (75 mL), dried (Na2SO4), and concentrated to give 3-bromo-5-chloro-2-fluoroaniline as a colorless oil which was carried forward without further purification: LCMS (m/z) 225.9 (MH+), tR=0.96 minute; 1H NMR (400 MHz, CDCl3) δ 6.88 (m, 1H), 6.70 (d, J=7.0 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859548B2
Source datasetuspto-grants-2014_10
ORD IDord-4d77d7bda2cd4b8191501cf56c0582c3
Source noteuspto-grants-2014_10