HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthalenemethanamine → HCID 18660163, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthalenemethanamine | HCID 8355 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 1,1-Dimethylethyl N-((1S,2S)-1-formyl-2-methylbutyl)carbamate | HCID 11390272 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 18660163 | HCID 18660163 | — |
Reaction Steps
To a slurry of 1-naphthylmethylamine (5.84 g, 37.2 mmol), crushed 3A molecular sieves (10 g), and N-t-butoxycarbonyl-isoleucinal (8.0 g, 37.2 mmol) in 1,2-dichloroethane (50 ml) was added sodium triacetoxyborohydride (15.8 g, 74.3 mmol) at 0° C. The reaction was allowed to warm slowly to RT and stirred for 48 hrs. The reaction was cooled to 0° C. and quenched with sat. aq. NaHCO3 and stirred for 30 min. The organic layer was separated, washed with saturated brine, dried (MgSO4) and evaporated in vacuo. The residue was purified by flash chromatography (SiO2, 25% ethyl acetate in hexanes) to provide the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05972984 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-754c1ed319be46359ceebe78b60c127e |
| Source note | uspto-grants-1999_10 |