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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197003Generated: October 31, 2026

2,6-Lutidine → HCID 22844258, compound

https://huagongshe.com/reaction/1197003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantTrimethylsilyl triflateHCID 65367—
ReactantHCID 22844257HCID 22844257—
SolventDichloromethaneHCID 6344—
ProductHCID 22844258HCID 22844258102.2%

Reaction Steps

To the solution of N-t-butoxycarbonyl-S-trityl-L-penicillamylglycine ethyl ester (B-2) (4.5 g) and 2,6lutidine (2.8 ml) in dichloromethane (100 ml), was added dropwise at 0° C. the solution of trimethylsilyl trifluoromethanesulfonate (3.9 ml), and the mixture was stirred for 1 hour while the temperature was gradually returned to the room temperature. To the reaction mixture was added ice-water, and the organic layer was washed with 1N-hydrochloric acid, water, an aqueous solution of sodium hydrogencarbonate, water, and saturated saline, in this order, and dried over magnesium sulfate. The solvent was evaporated off under reduced pressure, to give S-trityl-L-penicillamylglycine ethyl ester (3.8 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116861
Source datasetuspto-grants-1992_05
ORD IDord-d1a6480ba59a42bfa575cd52511f2274
Source noteuspto-grants-1992_05