HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 131715025, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 16219556 | HCID 16219556 | — |
| Reactant | HCID 131715026 | HCID 131715026 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 131715025 | HCID 131715025 | — |
| Product | HCID 131715026 | HCID 131715026 | — |
Reaction Steps
Boc-Phe-Gly-Ala-LeuCH2Cl was prepared by coupling Boc-Phe-Gly-Ala-OH (11.8 g, 30 mmol) to H-LeuCH2Cl.HCl (6.06 g, 30 mmol) using a mixed anhydride procedure. A mixed anhydride of Boc-Phe-Gly-Ala-OH was prepared in a solution of 300 mL of tetrahydrofuran and 25 mL of acetone, and then H-LeuCH2Cl HCl was added in acetone. The resulting crude product, 17.6 g, was dissolved in ether, treated with carbon, and filtered. Product Boc-Phe-Gly-Ala-LeuCH2Cl crystallized from ether (10.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04636492 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-c8b677167e63484aa1e6c461d8560173 |
| Source note | uspto-grants-1987_01 |