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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412162Generated: October 27, 2026

Triethylamine → 2.5-Di-[(methanesulfonyl)oxy]benzaldehyde

https://huagongshe.com/reaction/412162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2,5-DihydroxybenzaldehydeHCID 70949—
SolventDichloromethaneHCID 6344—
Product2.5-Di-[(methanesulfonyl)oxy]benzaldehydeHCID 18536186—

Reaction Steps

To a solution of 2,5-dihydroxybenzaldehyde (8.22 g, 59.5 mmol) in 100 mL of dichloromethane at 0° C. was added triethylamine (24.8 mL, 178 mmol), followed by dropwise addition of methanesulfonyl chloride (10.1 mL, 130 mmol). After 30 minutes, the solution was concentrated in vacuo, then partitioned between EtOAc and saturated NaHCO3 solution. The organic layer was washed with water and brine, dried (Na2SO4), filtered, and concentrated in vacuo. The product was isolated as a brown oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562823B1
Source datasetuspto-grants-2003_05
ORD IDord-5623e8b1669c443d8e97930d5d019eb5
Source noteuspto-grants-2003_05