HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthaldehyde → N-[2(S)-(t-Butoxycarbonylamino)-3(S)-methylpentyl]-N-(1-naphthylmethyl)glycine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthaldehyde | HCID 6195 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | N-(2(S)-(t-butoxycarbonylamino)-3(S)-methylpentyl)glycine methyl ester | HCID 10755806 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | N-[2(S)-(t-Butoxycarbonylamino)-3(S)-methylpentyl]-N-(1-naphthylmethyl)glycine methyl ester | HCID 10526565 | — |
Reaction Steps
N-[2 (S)-(t-Butoxycarbonylamino)-3 (S)-methylpentyl] glycine methyl ester (2.00 g, 6.97 mmol) was dissolved in 1,2dichloroethane (56 ml) and 3A molecular sieves were added followed by 1-naphthaldehyde (1.89 ml, 13.9 mmol) and sodium triacetoxyborohydride (6.65 g, 31.4 mmol). The mixture was stirred at ambient temperature for 16 h, filtered and evaporated in vacuo. The residue was partitioned between EtOAc (100 ml) and sat. aq. NaHCO3 (25 ml). The aqueous layer was extracted with EtOAc (3×50 ml). The organic extracts were combined, dried (Na2 SO4), filtered, and evaporated in vacuo to afford a residue which was purified by chromatography (SiO2, 15-33% ethyl acetate in hexanes) to afford the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05756528 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-3b957b0633a546d99ee25796ebf0b8d9 |
| Source note | uspto-grants-1998_05 |