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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358112Generated: October 25, 2026

Sulfuric Acid → 3-Bromo-2-fluorothioanisole

https://huagongshe.com/reaction/2358112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDimethyl DisulfideHCID 12232—
Reactant1-Bromo-2-fluorobenzeneHCID 61259—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-2-fluorothioanisoleHCID 5744806450%

Reaction Steps

To a solution of 1-bromo-2-fluorobenzene (2.0 g, 11.4 mmol) in dry tetrahydrofuran (50 ml) under nitrogen, at −78° C. was added lithium diisopropylamide (2.5 M in hexane, 6.28 ml, 15.4 mmol). The mixture was stirred for 5 minutes after which dimethyldisulfide (0.92 ml, 15.4 mmol) was added and the stirring was continued at −78° C. for an additional hour. The reaction mixture was brought to ambient temperature and aqueous sulfuric acid (10%, 50 ml) was added. The phases were separated and the aqueous phase extracted with ethylacetate (3×100 ml). The combined organic phases was dried (MgSO4) and evaporated to dryness to give an oil. The residue was purified by flash column chromatography (isooctane) to give the title compound (1.26 g). MS m/z (relative intensity, 70 eV) 222 (M+, bp), 220 (M+, 91), 189 (24), 187 (25), 126 (97).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763639B2
Source datasetuspto-grants-2010_07
ORD IDord-1ed124e1cc9f4c6dbe5a76f5c4e55152
Source noteuspto-grants-2010_07