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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911714Generated: November 2, 2026

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

https://huagongshe.com/reaction/911714

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 numberUS08022062B2
Source datasetuspto-grants-2011_09
ORD IDord-56f1bd56b1764cbb81f5aa48614e6ce7
Source noteuspto-grants-2011_09