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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831489Generated: October 31, 2026

Hydrochloric Acid → 2-Chloro-5-fluoro-4-methoxyaniline

https://huagongshe.com/reaction/1831489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Chloro-4-fluoro-5-methoxy-2-nitrobenzeneHCID 22052046—
SolventWaterHCID 962—
Product2-Chloro-5-fluoro-4-methoxyanilineHCID 22052070186.7%

Reaction Conditions

Temperature55 °C

Reaction Steps

1-Chloro-4-fluoro-5-methoxy-2-nitro-benzene (16.3 g, 79.3 mmol) and Sn granules (29.1 g, 246 mmol) were suspended in water (200 mL). Concentrated HCl (79 mL, 952 mmol) was added dropwise over 20 min. The resulting mixture was heated to 55° C. for 3 h. The solution was cooled to room temperature and carefully quenched with 1 N NaOH. The thick mixture was filtered through celite eluting the ethyl acetate to give a clear solution which was extracted with ethyl acetate. The ethyl acetate layers were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo to give 26 g (80%) of 2-chloro-5-fluoro-4-methoxyaniline: Crude 1H NMR (400 MHz, CDCl3): δ 6.88 (d, J=8.3 Hz, 1H), 6.57 (d, J=12.2 Hz, 1H), 3.79 (s, 3H), 3.77 (br s, 2H). The crude material was pure enough to carry on to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067658B2
Source datasetuspto-grants-2006_06
ORD IDord-be493efc37c44551aee5efabc7654a20
Source noteuspto-grants-2006_06