HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-tert-Butyl 2-((benzyloxy)methyl)morpholine-4-carboxylate → (R)-N-Boc-2-hydroxymethylmorpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-tert-Butyl 2-((benzyloxy)methyl)morpholine-4-carboxylate | HCID 53989854 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-N-Boc-2-hydroxymethylmorpholine | HCID 1512576 | 99.2% |
Reaction Steps
To a solution of (R)-tert-butyl 2-(benzyloxymethyl)morpholine-4-carboxylate (8.33 g, 27.1 mmol) in EtOH was added Pd—C (wet, 3.6 g), and the resulting mixture was stirred at rt under a H2 balloon overnight. After filtration, the solvent was removed under vacuum, and the residue was purified by flash column chromatography to give (R)-tert-butyl 2-(hydroxymethyl)morpholine-4-carboxylate (5.84 g, 99%) as a clear oil. 1H NMR (400 MHz, CDCl3): 3.88 (d, 2 H), 3.82 (br, 1 H), 3.64 (d, 1 H), 3.56 (m, 3 H), 2.94 (m, 1 H), 2.76 (m, 1 H), 1.90 (br, 1 H), 1.44 (s, 9 H); MS m/z 218 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08455521B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-0940eccb73e24e31879f8005dab3df0f |
| Source note | uspto-grants-2013_06 |