HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Naphthol → HCID 13188829, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Naphthol | HCID 8663 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]- | HCID 77857 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13188829 | HCID 13188829 | — |
Reaction Steps
6.2 g of dicyclohexylcarbodiimide are added to a solution of 7.8 g of tert.-butyoxycarbonyl-L-phenylalanine and 5.3 g of β-naphthol in 50 ml of absolute tetrahydrofurane at 0° C. and the reaction mixture was kept at 4° C. for 12 hours. The dicyclohexylurea which had precipitated was then separated off by filtration and the filtrate was evaporated to dryness in vacuo. The crystalline residue was recrystallised twice from ethyl acetate/cyclohexane and finally from acetonitrile. 8.5 g (73% of theory) of melting point 118°-119° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04239902 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-19f3b825e0dd496b98c9e5f8d7860e5d |
| Source note | uspto-grants-1980_12 |