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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229738Generated: October 30, 2026

Water → 2-Bromo-1-fluoro-4-nitrobenzene

https://huagongshe.com/reaction/229738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantBromineHCID 24408—
CatalystHCID 178418844HCID 178418844—
SolventDichloromethaneHCID 6344—
Product2-Bromo-1-fluoro-4-nitrobenzeneHCID 6969970%

Reaction Conditions

Temperature10 °C

Reaction Steps

In a 20 L 4-necked RB flask, fitted with a mechanical stirrer, reflux condenser, add DM water (550 ml), conc. Sulphuric acid (6.2 L, 113 M), 4-fluronitrobenzene(1.0 kg, 7.09 M) at 25-35° C. under stirring. The reaction mixture was cooled to 10° C. and bromine (1.13 kg, 7.06 M) was added to reaction mixture under stirring. The reaction mixture was brought to temp. 25-35° C., silver sulfate (1.1 kg, ˜3.53 M) was added in one portion to the reaction mixture at 25-35° C. and maintained for 30-32 h under stirring. Monitor the progress of the reaction by GC and after ascertaining completion, the reaction mixture was poured slowly into ice cold water (12 L) and dichloromethane (12 L) mixture. Filter the insoluble and wash the inorganic with dichloromethane (2 L). Combine the organic layer, wash with 10% sodium bicarbonate (3 L), water (5 L). The dichloromethane layer was distilled below 40° C. under vacuum and add n-Hexane (4.5 L) to the residue. The resulting mass was stirred at 25-35° C. for 4-5 hr, filter the product and dried in vacuum oven below 35° C. till LOD reaches <1%. The dried product appears as white lustrous crystalline solid, weighs about 1.1-1.2 kg, yield 70-77%, purity 97-98% by HPLC, m.p. 56-58° C. The structure assigned to the product is in agreement with spectral data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563900B2
Source datasetuspto-grants-2009_07
ORD IDord-ccbb49cd89154c0daf69baea16d3f105
Source noteuspto-grants-2009_07