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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041577Generated: November 2, 2026

Triethylamine → 2-Methanesulfonyloxymethyl-5-(3-methyl-butyryl)-pyridine

https://huagongshe.com/reaction/2041577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Hydroxymethyl-5-(3-methyl-butyryl)-pyridineHCID 57656417—
SolventDichloromethaneHCID 6344—
Product2-Methanesulfonyloxymethyl-5-(3-methyl-butyryl)-pyridineHCID 5765658798.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolve 2-hydroxymethyl-5-(3-methyl-butyryl)-pyridine (190 mg, 0.98 mmol) in dichloromethane (10 mL). Cool to 0° C. and add triethylamine (0.151 mL, 1.08 mmol) and methanesulfonyl chloride (0.083 mL, 1.08 mmol). Allow the mixture to warm to room temperature and stir for 2 h. Dilute the reaction mixture with dichloromethane and wash with saturated aqueous NaHCO3. Dry the organic phase over Na2SO4, filter and concentrate in vacuo to provide the title compound as oil (263 mg, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580780B2
Source datasetuspto-grants-2013_11
ORD IDord-77704a653be445cca9057efc36232bac
Source noteuspto-grants-2013_11