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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369576Generated: October 28, 2026

1-Chloro-2-fluorobenzene → 1-Chloro-2-fluoro-3-(methylsulfanyl)benzene

https://huagongshe.com/reaction/369576

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2-fluorobenzeneHCID 9583—
ReactantDimethyl DisulfideHCID 12232—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-Chloro-2-fluoro-3-(methylsulfanyl)benzeneHCID 17859825—

Reaction Steps

A solution of 10 g (grams) (76 mmol (millimoles)) of 1-chloro-2-fluorobenzene in 75 mL (milliliters) of dry tetrahydrofuran (THF) was cooled with a dry ice/acetone bath and 34 mL (84 mmol) of 2.5M butyllithium was added dropwise under a nitrogen blanket over 45 min with stirring and cooling. The resulting solution was stirred for 2 hours at -78° C. A solution of 8.1 mL (91 mmol) of dimethyl disulfide in 10 mL of dry THF was added with stirring over a 30-min period keeping the temperature below -65° C. The mixture was allowed to warm to ambient temperature for 1 hour. It was then diluted with 75 mL of water. The resulting mixture was extracted with diethyl ether and the ether extract was dried over sodium sulfate and concentrated by evaporation under reduced pressure to obtain a yellow oil. This oil was purified by flash chromatography on 230-400 mesh silica gel eluting with a hexane/ethyl acetate mixture to obtain 9.0 g (69 percent of theory) of the title compound as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140271
Source datasetuspto-grants-2000_10
ORD IDord-b0ee5de67ce845d08ab6f2eb1edd7594
Source noteuspto-grants-2000_10