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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116469Generated: October 30, 2026

3-Bromobenzene-1-sulfonyl fluoride → Benzene, 1-bromo-3-(phenylsulfonyl)-

https://huagongshe.com/reaction/2116469

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromobenzene-1-sulfonyl fluorideHCID 70700039—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
ProductBenzene, 1-bromo-3-(phenylsulfonyl)-HCID 64092088%

Reaction Steps

To a stirred solution of 3-bromophenylsulfonyl fluoride (D1) (1 g, 4.18 mmol) in dry THF (20 ml) at −78° C., under argon was added phenylmagnesium bromide (1 M, 1.4 ml, 4.18 mmol) dropwise. The reaction was left to warm to room temperature overnight and then quenched with ammonium chloride (50 ml), extracted with ethyl acetate (3×40 ml) and the combined organic extracts dried (Na2SO4). Solvents were evaporated in vacuo to give a colourless solid (1.09 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439245B2
Source datasetuspto-grants-2008_10
ORD IDord-5610c6111bc84816b02a1c2e998d54b3
Source noteuspto-grants-2008_10