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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238899Generated: October 31, 2026

HCID 69032396, compound → HCID 86605613, compound

https://huagongshe.com/reaction/238899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69032396HCID 69032396—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 86605613HCID 8660561341%

Reaction Steps

4-Benzyloxy-1,2,3-tri(tert-butyldimethylsilyloxy)-L-threitol (5.9 g, 10.6 mmol) dissolved in EtOAc (70 mL) was hydrogenated (balloon as H2 container) in the presence of 10% Pd/C (1 g) until no more starting material could be detected on TLC plate (about 5 h). The catalyst was removed by filtration through a Celite pad, with rinsing the solid with EtOAc. The filtrate was evaporated to dryness, and the residue was purified by silica gel flash chromatography (eluting with 10% ether in hexanes) to give 1,2,3-tri(tert-butyldimethylsilyloxy)-L-threitol (2.1 g, 41% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642644B2
Source datasetuspto-grants-2014_02
ORD IDord-53a2ae337fba4f959c2af386a58f80c0
Source noteuspto-grants-2014_02