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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904446Generated: October 27, 2026

2,6-Lutidine → N-(t-Butyldimethylsilyloxycarbonyl)-L-methionine methyl ester

https://huagongshe.com/reaction/1904446

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
Reactant(S)-Methyl 2-((tert-butoxycarbonyl)amino)-4-(methylthio)butanoateHCID 11097398—
SolventDichloromethaneHCID 6344—
ProductN-(t-Butyldimethylsilyloxycarbonyl)-L-methionine methyl esterHCID 13934327—

Reaction Steps

To a methylene chloride solution (1.0 ml) of N-t-butoxycarbonyl-L-methionine methyl ester (131.5 mg, 0.5 mmol) and 2,6-lutidine (0.116 ml, 1.0 mmol), t-butyldimethylsilyltrifluoromethane sulfonate (TBDMSOTf) (0.172 ml, 0.75 mmol) was added dropwise at room temperature in a nitrogen atmosphere. After the mixture was stirred for 15 minutes, a saturated aqueous solution of ammonium chloride (2 ml) was added to quench the reaction and extraction with ether was conducted. The organic layer was dried over anhydrous magnesium sulfate and filtered. By distilling off the solvent under vacuum, the titled compound was obtained in an amount of 146 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837349
Source datasetuspto-grants-1989_06
ORD IDord-54293b7aebdf400ea2dde9437087daa5
Source noteuspto-grants-1989_06