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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254307Generated: November 1, 2026

(R)-tert-Butyl 2-((benzyloxy)methyl)morpholine-4-carboxylate → (R)-N-Boc-2-hydroxymethylmorpholine

https://huagongshe.com/reaction/1254307

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-tert-Butyl 2-((benzyloxy)methyl)morpholine-4-carboxylateHCID 53989854—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(R)-N-Boc-2-hydroxymethylmorpholineHCID 151257699.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455521B2
Source datasetuspto-grants-2013_06
ORD IDord-0940eccb73e24e31879f8005dab3df0f
Source noteuspto-grants-2013_06