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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365217Generated: October 31, 2026

Sulfuric Acid → 1-Azido-4-fluorobenzene

https://huagongshe.com/reaction/2365217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-FluoroanilineHCID 9731—
ReactantSodium AzideHCID 33557—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product1-Azido-4-fluorobenzeneHCID 1088797496.5%

Reaction Steps

Prepared in analogy to J. Org. Chem. (1989) 54:5938-5945. To a solution of sulfuric acid (40 mL) and trifluoroacetic acid (200 mL) was added 4-fluoroaniline (22.1 mL, 0.23 mol) dropwise. Then under ice-cooling a solution of sodium nitrite (20.6 g, 0.3 mol) in water (200 mL) was added over 30 min at 15-18° C. The solution was then stirred for 30 min while kept in the ice bath. A solution of sodium azide (25.42 g, 0.39 mol) in water (150 mL) was added dropwise over 30 min. Mixture was foaming and temperature went up to 10° C. while cooling with an ice bath. Reaction mixture was stirred without cooling for 1 h, then extracted with diethyl ether. The combined organic layers were washed with water two times. Then the combined organic layers were diluted with saturated aqueous sodium carbonate solution (500 mL) until the mixture became basic. The organic phase was separated and washed with brine, extracted again with diethyl ether. The organic layers were dried over sodium sulfate and evaporated at 40° C., minimum 50 mbar (already distillation of product), to afford the title product (30.42 g, 96%) as a brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697696B2
Source datasetuspto-grants-2014_04
ORD IDord-7bd23a7b78ee4ed99cfdf5a84f7bae67
Source noteuspto-grants-2014_04