HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Leu-Pro-OBn
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Boc-Leu-Pro-OBn | HCID 10093486 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Leu-Pro-OBn | HCID 10663366 | — |
Reaction Steps
To a flask containing Boc-Leu-Pro-OBn (113.8 g, 272 mmol) a solution of hydrogen chloride in dioxane (209 ml, 5.3 N) was added and the stirring was continued for 5 h or until total conversion by TLC (disappearance of starting material; Rf=0.47 (hex-EtOAc 2:1, silica). The solution was concentrated under reduced pressure and the resulting oil was chased with CHCl3 (3×50 ml), CHCl3-MTBE (30 ml-50 ml), MTBE (50 ml) and hex (50 ml). The residue was dried under vacuum (16 h) to remove residual HCl, to give the title compound as a white solid. A5 (96.4 g, 100%) was used directly without further purification in the next step. [α]D22−85.21 (c=1, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07348310B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-e8778ed70d4f4f88a012c9dab199b19b |
| Source note | uspto-grants-2008_03 |