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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227534Generated: November 3, 2026

Hydrochloric Acid → 3-Fluoro-4-methylanisole

https://huagongshe.com/reaction/2227534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrafluoroboric acidHCID 28118—
Reactant5-Methoxy-o-toluidineHCID 99500—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product3-Fluoro-4-methylanisoleHCID 277457131%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 5-methoxy-2-methyl aniline (5.0 g; 36 mmol), HCl (7.6 mL of a 12 M solution; 91 mmol) and H2O (11 mL) was heated at 60° C. for 15 min until complete dissolution had occurred. The reaction was cooled to 0° C. and an aqueous solution of NaNO2 (2.5 g; 36 mmol) was added dropwise (internal temperature ≦7° C.). The reaction was stirred at 0° C. for 30 min and a 0° C. solution of HBF4 (5.3 mL of a 48% solution; 40 mmol) was added cautiously. The reaction was stirred at 0° C. for 20 min, and the resultant brown solid was filtered, washed with ice water (3×10 mL) and H2O (2×10 mL). The solid was dried under high vacuum for 20 h, then heated (heat gun) until evolution of BF3 (white fumes) had ceased. The resulting brown oil was partitioned between EtOAc and H2O. The organic phase was dried (Na2SO4), concentrated in vacuo and distilled by Kugelrohr to give 3-fluoro-4-methyl anisole (1.6 g; 31%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414002B1
Source datasetuspto-grants-2002_07
ORD IDord-cecd534b5b2849ea9b72b313877672af
Source noteuspto-grants-2002_07