Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197004Generated: October 31, 2026

Acetyl chloride → HCID 22844246, compound

https://huagongshe.com/reaction/1197004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 22844258HCID 22844258—
SolventDichloromethaneHCID 6344—
ProductHCID 22844246HCID 22844246—

Reaction Steps

To the solution of S-trityl-L-penicillamylglycine ethyl ester (C-2) (3.7 g) in dichloromethane (50 ml) were added acetyl chloride (0.66 ml) and triethylamine (0.88 ml) at 0° C. The mixture was stirred at the same temperature for 15 minutes and then ice water was added. The organic layer was washed with an aqueous potassium hydrogensulfate solution, water, an aqueous sodium hydrogencarbonate solution, water and saturated saline, in this order, and dried over magnesium sulfate. The solvent was evaporated off under reduced pressure, and the residue was subjected to silica gel column chromatography, to give N-acetyl-S-trityl-L-penicillamylglycine ethyl ester (3.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116861
Source datasetuspto-grants-1992_05
ORD IDord-b587c44a231e4794a17abbe3d270a03f
Source noteuspto-grants-1992_05