Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889236Generated: October 26, 2026

Ethyl Acetate → 2-Methanesulfonyloxy-5-methylbenzoic acid methyl ester

https://huagongshe.com/reaction/889236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantMethyl 5-methylsalicylateHCID 89802—
SolventTetrahydrofuranHCID 8028—
Product2-Methanesulfonyloxy-5-methylbenzoic acid methyl esterHCID 86638979—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a ice cooled suspension of sodium hydride (60%, 1.3 g, 78.3 mmol) in THF (100 mL) is added a solution of 2-hydroxy-5-methylbenzoic acid methyl ester (10 g, 60 mmol) in THF (20 mL) and it is stirred at 0° C. Then a solution of methanesulfonyl chloride (8.2 g, 72 mmol) in THF (20 mL) is added dropwise. The reaction mixture is stirred at RT for 18 h. Then the reaction mixture is cooled in an ice bath and slowly ice is added to quench the reaction. EtOAc is used to extract. Brine is added to the aqueous phase and re-extracted with EtOAc. The combined organic phase is washed with water, brine, dried over NaSO4 and MgSO4, and concentrated to give the title compound as an oil. It is used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252820B2
Source datasetuspto-grants-2012_08
ORD IDord-bfd77a7eb4ed4c36bd2f27f4462f51ec
Source noteuspto-grants-2012_08