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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157446Generated: November 2, 2026

Triethylamine → 2-Acetylamino-5-(3-methanesulfonyloxypropoxy)benzoic acid methyl ester

https://huagongshe.com/reaction/1157446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Acetylamino-5-(3-hydroxypropoxy)benzoic acid methyl esterHCID 68521549—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-Acetylamino-5-(3-methanesulfonyloxypropoxy)benzoic acid methyl esterHCID 86622903—

Reaction Steps

To a solution of 2-acetylamino-5-(3-hydroxypropoxy)benzoic acid methyl ester (689 mg, 2.6 mmol) in dichloromethane (25 mL) cooled to 0° C. were added methanesulfonyl chloride (1 mL, 12.9 mmol) and triethylamine (3.6 mL, 25.8 mmol). The mixture was warmed to room temperature and stirred for 2.5 h. The mixture was diluted with ethyl acetate (100 mL) and washed with 1 N HCl (aq.) (1×50 mL), sat. NaHCO3 (aq.) (1×50 mL) and brine (1×50 mL). The organic layer was dried (MgSO4), filtered and concentrated in vacuo. Crude 2-acetylamino-5-(3-methanesulfonyloxypropoxy)benzoic acid methyl ester thus obtained was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807686B2
Source datasetuspto-grants-2010_10
ORD IDord-8a18c6b5825c4fe08ce63b558d4ce838
Source noteuspto-grants-2010_10