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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046657Generated: November 2, 2026

Sodium Hydroxide → 1-Bromo-3-(methanesulfonyl)-5-methylbenzene

https://huagongshe.com/reaction/1046657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3,5-DibromotolueneHCID 15361—
ReactantL-ProlineHCID 145742—
ReactantSodium methanesulfinateHCID 2733271—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
Product1-Bromo-3-(methanesulfonyl)-5-methylbenzeneHCID 5925129860.2%

Reaction Conditions

Temperature210 °C

Reaction Steps

A mixture of 3,5-dibromotoluene (2.0 g, 8.0 mmol), sodium methanesulfinate (0.92 g, 9.0 mmol), copper(I) iodide (152 mg, 0.8 mmol), proline (0.18 g, 1.6 mmol) and sodium hydroxide (64 mg, 1.6 mmol) in DSMO (15 mL, anhyd) was heated in a microwave unit (Biotage Initiator™) at 210° C. for min. The reaction was repeated two more times and the reaction mixtures were combined, diluted with H2O and extracted with EtOAc. The combined extracts were washed with H2O and brine, then dried (Na2SO4), concentrated and purified by chromatography (silica, EtOAc/Hex, 0:100 to 40:60) to give the title compound (1.2 g, 20% combined yield) as a white solid. GC-MS (EI): 248, 250.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569352B2
Source datasetuspto-grants-2013_10
ORD IDord-49b080aaef34439895cd5e9145f0a8ff
Source noteuspto-grants-2013_10