HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → benzyl N-acetyl-(L)-pyroglutamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzyl 5-oxoprolinate | HCID 2381219 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | benzyl N-acetyl-(L)-pyroglutamate | HCID 13655552 | — |
Reaction Steps
A solution of 61.3 g (280 mmol) of benzyl (L)-pyroglutamate in 400 ml of benzene is added over 2 hours to a suspension of 13.4 g of NaH (280 mmol) in 50 ml of dry benzene. After stirring for one hour at ordinary temperature, a solution of 22.7 g (290 mmol) of acetyl chloride in 150 ml of benzene is run in and the mixture is heated at 55° for 5 hours and then stirred for 24 hours at ordinary temperature, washed with 2×150 ml of water, dried and evaporated. The product is distilled under reduced pressure; boiling point=150°-60° C. (0.25 mm Hg). This gives 60% of a pure product of Rf=0.63 (A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04661512 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-1ff4797f5c944570a36e8a6a136700e8 |
| Source note | uspto-grants-1987_04 |