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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926943Generated: October 26, 2026

Methanol → (Fluoromethanesulfinyl)benzene

https://huagongshe.com/reaction/926943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-bromobutanimideHCID 67184—
ReactantFluoromethyl phenyl sulfideHCID 5314298—
SolventWaterHCID 962—
Product(Fluoromethanesulfinyl)benzeneHCID 32513389.6%

Reaction Steps

Fluoromethyl phenyl sulphide (85 g, 351.63 mmol) was added to a mixture of methanol (250 ml) and water (50 mL). The resulting mixture was cooled to a temperature between 0° C. and 5° C. NBS (75.10 g, 1.2 eq) was added in small portions maintaining the same temperature range. The reaction mixture was stirred until the reaction was complete, and then, was quenched with Na2SO3 solution (10%, 150 mL). The pH of the reaction mixture was adjusted to a value between 7 and 8 with NaHCO3 saturated solution. The mixture was concentrated under vacuum at a temperature between 20° C. and 25° C. The residue was extracted with dichloromethane (200 mL, 300 mL). The combined organic layer was washed with water (2×300 mL) and concentrated to ⅓ of the volume. Heptane (50 mL) was added and the resulting mixture was concentrated again. The crude product was purified by flash chromatography (Ethyl Acetate/Hexane 30:70) to give 49.8 g (89.6%) of the desired product as colourless oil at rt, which is a white solid at −20° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290446B2
Source datasetuspto-grants-2016_03
ORD IDord-f5d67237b7de4b049dbb2caebd939497
Source noteuspto-grants-2016_03