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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859698Generated: November 1, 2026

Methyl iodide → 4-Bromo-2-chloro-1-methanesulfonylbenzene

https://huagongshe.com/reaction/859698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium AcetateHCID 517045—
Reactant4-Bromo-2-chlorobenzenesulfonyl chlorideHCID 2734766—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-2-chloro-1-methanesulfonylbenzeneHCID 2309306132.4%

Reaction Steps

Hydrazine monohydrate (1.51 mL, 48 mmol) was added to a cooled 0° C. solution of 4-bromo-2-chlorobenzenesulfonyl chloride (5 g, 17.2 mmol) dissolved in THF (50 mL). The reaction was stirred at room temperature for 2 hours and then the solvent was removed in vacuo to give a white solid. The solid was dissolved in EtOH (100 mL) and treated with sodium acetate (6.56 g, 80 mmol) followed by methyl iodide (4.9 mL, 79 mmol). The reaction mixture was refluxed for 18 hours. The solvent was removed in vacuo to give a residue that was partitioned between 1 N HCl and EtOAc. The organic layer was dried over MgSO4 and concentrated. The crude mixture was purified by flash column chromatography to give the product (1.5 g, 32%). 1H NMR (300 MHz, CDCl3): δ 3.26 (s, 3 H), 7.63 (dd, J=8.5, 1.9 Hz, 2 H), 7.74 (d, J=1.9 Hz, 1 H), 8.02 (d, J=8.5 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07151105B2
Source datasetuspto-grants-2006_12
ORD IDord-dea5459c89034b29a8ef6b3c3fdfb9d9
Source noteuspto-grants-2006_12