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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904444Generated: October 31, 2026

2,6-Lutidine → HCID 14765842, compound

https://huagongshe.com/reaction/1904444

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
ReactantN-Boc-allylglycine methyl esterHCID 22243128—
SolventDichloromethaneHCID 6344—
ProductHCID 14765842HCID 14765842—

Reaction Steps

To a methylene chloride solution (1.5 ml) of N-(t-butoxycarbonyl)-allylglycine methyl ester (183 mg, 0.8 mmol) and 2,6-lutidine (0.186 ml, 1.6 mmol) was added t-butyldimethylsilyltrifluoromethane sulfonate (TBDMSOTf) (0.275 ml, 1.2 mmol) at room temperature in a nitrogen atmosphere. After the mixture was stirred for 15 minutes, a saturated aqueous solution of ammonium chloride (3 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 260 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837349
Source datasetuspto-grants-1989_06
ORD IDord-9ddae1b29bce4278a1064e3de9d1ce72
Source noteuspto-grants-1989_06