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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878299Generated: October 30, 2026

Sodium hydride → Methyl 3-chloro-5-(methylsulfonyl)benzoate

https://huagongshe.com/reaction/878299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantL-ProlineHCID 145742—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium methanesulfinateHCID 2733271—
ReactantMethyl 3-chloro-5-iodobenzoateHCID 24721134—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-chloro-5-(methylsulfonyl)benzoateHCID 18952494—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of L-proline (77.7 mg, 675 μmol) in DMSO (4 mL) was added sodium hydride (27.0 mg, 675 μmol, 60% dispersion in mineral oil) and the mixture was stirred at room temperature for 30 minutes before copper(I)iodide (128 mg, 675 μmol), methyl 3-chloro-5-iodobenzoate (0.25 g, 843 μmol) and sodium methanesulfinate (689 mg, 6.75 mmol) were added. The reaction mixture was heated to 120° C. in a sealed tube to give a turbid blue solution. After 2 hours the reaction mixture was allowed to cool down and was poured on saturated aqueous NaHCO3 solution and EtOAc and filtered. The filtrate layers were separated and the aqueous layer was extracted twice with EtOAc. The organic layers were washed once with brine, dried over MgSO4, filtered and evaporated. Light brown solid (0.135 g; 64%). MS (EI): m/z=248 [M].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987307B2
Source datasetuspto-grants-2015_03
ORD IDord-c87a3e579f3b4936b0f60b9d2586a583
Source noteuspto-grants-2015_03