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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043698Generated: November 1, 2026

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

https://huagongshe.com/reaction/1043698

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 numberUS08563553B2
Source datasetuspto-grants-2013_10
ORD IDord-d1c1705945b44971a8bdfe1f7d31ea8a
Source noteuspto-grants-2013_10