HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 22844246, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 22844258 | HCID 22844258 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22844246 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05116861 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-b587c44a231e4794a17abbe3d270a03f |
| Source note | uspto-grants-1992_05 |