Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849558Generated: October 25, 2026

Sulfuric Acid → 5-Bromo-2-fluoro-1,3-dimethylbenzene

https://huagongshe.com/reaction/849558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTetrafluoroboric acidHCID 28118—
Reactant4-Bromo-2,6-xylidineHCID 90549—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product5-Bromo-2-fluoro-1,3-dimethylbenzeneHCID 273629872%

Reaction Steps

To a mixture of 4-Bromo-2,6-dimethylaniline (8.3 g, 42 mmol) at 5° C. and H2O (50 mL) was added conc H2SO4 (6.25 mL). NaNO2 (4.1 g) was added in portions until an excess was indicated by starch iodide paper. Water (30 mL) was added to make the mixture homogeneous. After transferring to a plastic container, HBF4 (50%, 13.7 g) was added dropwise with stirring. The resultant white precipitate was collected by vacuum filtration, washed with H2O (30 mL), MeOH (30 mL), and Et2O (60 mL), and dried over P2O5 under vacuum for 16 h. The solid was then heated in a glass flask with an open flame until all the solid had decomposed. The remaining liquid was diluted with Et2O (50 mL) and 0.5 M NaOH (30 mL). The organic layer was separated, washed with 0.5 M NaOH (25 mL), H2O (25 mL), brine (25 mL), dried (MgSO4), and concentrated in vacuo yielding 6.06 g (72%) of 1-bromo-4-fluoro-3,5-dimethylbenzene as a pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06013652
Source datasetuspto-grants-2000_01
ORD IDord-c23e18ac3014424a98269e671b0fb27e
Source noteuspto-grants-2000_01