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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904445Generated: October 30, 2026

2,6-Lutidine → N-t-butyldimethylsilyloxycarbonylvaline methyl ester

https://huagongshe.com/reaction/1904445

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
ReactantN-(tert-Butoxycarbonyl)-L-valine methyl esterHCID 11031717—
SolventDichloromethaneHCID 6344—
ProductN-t-butyldimethylsilyloxycarbonylvaline methyl esterHCID 13934325—

Reaction Steps

To a methylene chloride solution (1.0 ml) of N-t-butoxycarbonyl-L-valine methyl ester (115.5 mg, 0.5 mmol) and 2,6-lutidine (0.116 ml, 1.0 mmol) was added dropwise t-butyldimethylsilyltrifluoromethane sulfonate (0.172 ml, 0.75 mmol) 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 153.2 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837349
Source datasetuspto-grants-1989_06
ORD IDord-b943ef89acb54ada8861d8394caf3533
Source noteuspto-grants-1989_06