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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911717Generated: November 2, 2026

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

https://huagongshe.com/reaction/911717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant5-Hydroxymethyl-2-(3-methyl-butyryl)-pyridineHCID 57656192—
SolventDichloromethaneHCID 6344—
Product5-Methanesulfonyloxymethyl-2-(3-methyl-butyryl)-pyridineHCID 5765634587%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolve 5-hydroxymethyl-2-(3-methyl-butyryl)-pyridine (210 mg, 1.086 mmol) in dichloromethane (5 mL). Cool to 0° C. and add triethylamine (0.167 mL, 1.195 mmol) and methanesulfonyl chloride (0.093 mL, 1.195 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 (256 mg, 87%). GC-MS m/z: 271

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022062B2
Source datasetuspto-grants-2011_09
ORD IDord-8ca9c1eb03f64ec6b05e45aabb6f1235
Source noteuspto-grants-2011_09