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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217638Generated: October 27, 2026

Triethylamine → 4-Methanesulfonyloxymethylbenzoic acid benzyl ester

https://huagongshe.com/reaction/217638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzyl 4-(hydroxymethyl)benzoateHCID 15650225—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
Product4-Methanesulfonyloxymethylbenzoic acid benzyl esterHCID 5800121373%

Reaction Steps

Under ice cooling, methanesulfonyl chloride (2.1 mL, 27 mmol) was added to a solution of 4-hydroxymethylbenzoic acid benzyl ester (Reference Compound No. 7-1, 6.0 g, 24.8 mmol) and triethylamine (7.6 mL, 54 mmol) in dichloromethane (60 mL), and then the reaction mixture was stirred at room temperature for 50 minutes. Brine (0.30 L) was added to the reaction solution, and the mixture was extracted with chloroform (0.15 L) four times. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give 5.8 g of the title reference compound as yellow oil. (Yield 73%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198271B2
Source datasetuspto-grants-2012_06
ORD IDord-6e50367ecbe24a3ab19eadf2abc741fe
Source noteuspto-grants-2012_06