HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dl-Phenylalanine → 1170-76-9
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dl-Phenylalanine | HCID 994 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Benzyloxycarbonylglycine | HCID 14349 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1170-76-9 | HCID 70889 | 70.2% |
Reaction Steps
A solution of 4.2 g (0.02 mole) of N-carbobenzoxyglycine and 2.2 g (0.022 mole) of N-methylmorpholine in 50 ml of dry toluene was cooled to -5° and 2.8 g (0.02 mole) of isobutyl chloroformate was added thereto. After 1 hour, a solution of 3.3 g (0.02 mole) of DL-phenylalanine in 20 ml of N-sodium hydroxide was added and the mixture was stirred vigorously overnight. The aqueous phase was isolated, extracted with ether and acidified with 4 N Hydrochloric acid to precipitate the product as a colorless oil which crystallized upon cooling. Recrystallization from ethanol-water yielded 5 g (70%) of N-carbobenzoxyglycyl-DL-phenylalanine, mp 158°-160° C., RfA 0.61.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04261884 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-12ace38ffe294a6d9403db58f591ad29 |
| Source note | uspto-grants-1981_04 |