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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410139Generated: October 25, 2026

Hydrochloric Acid → (2-Fluoro-4-methoxyphenyl)hydrazine

https://huagongshe.com/reaction/1410139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium NitriteHCID 23668193—
Reactant2-Fluoro-4-methoxyaniline hydrochlorideHCID 44784928—
SolventWaterHCID 962—
Product(2-Fluoro-4-methoxyphenyl)hydrazineHCID 4420304538.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a vigorously stirred suspension of 2-fluoro-4-methoxyaniline hydrochloride (665 mg, 3.7 mmol) in cone. HCl (5.5 mL) cooled to 0° C. was added a cold solution of NaNO2 (312 mg, 4.5 mmol) in H2O (1 mL). The mixture was stirred at 0° C. for 90 min. A cold solution of SnCl2-2H2O (3.4 g, 15.0 mmol) in cone. HCl (5.5 mL) was then added slowly to the solution of diazonium salt. The reaction was allowed to warm to room temperature, stirred for 30 min and the reaction was filtered. The collected precipitate was washed on the filter with several large portions of ether and dried under vacuum. The solid was dissolved in DCM and washed saturated NaHCO3, extracted and dried using a phase separator. Evaporation gave (2-fluoro-4-methoxyphenyl) hydrazine (220 mg 38%), which was used in the next step without further purification. The procedure was adapted from J. Med. Chem. 2000, 43, 4701.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921402B2
Source datasetuspto-grants-2014_12
ORD IDord-ab5fe922e63c401e8d47f587f3c24a05
Source noteuspto-grants-2014_12