HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2S,3S)-2-(N-Benzyloxycarbonylamino)-3-octadecanol → (2S,3S)-2-Amino-3-octadecanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2S,3S)-2-(N-Benzyloxycarbonylamino)-3-octadecanol | HCID 58743388 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2S,3S)-2-Amino-3-octadecanol | HCID 57017700 | 89% |
Reaction Steps
To a solution of N-benzyloxycarbonylamine 90 (330 mg, 0.79 mmol) in MeOH (40 mL) at room temperature, Pd—C (10% wt, 100 mg, 0.09 mmol) was added. The mixture was purged with a stream of dry Ar, and then H2. The reaction was stirred overnight under a H2 atmosphere (1 atm). The catalyst was filtered off through a 0.45 μm teflon filter in polypropylene housing, washing the filter with MeOH (50 mL) and the solvent was evaporated in vacuo. The crude was purified by column chromatography on silica (90:10 CH2Cl2/MeOH to 100% MeOH) to obtain aminoalcohol 91 as a white solid (200 mg, 89% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138547B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-83630ad523ed493bb455ccf9435fdefb |
| Source note | uspto-grants-2006_11 |