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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409799Generated: October 30, 2026

HCID 66622747, compound → HCID 66622302, compound

https://huagongshe.com/reaction/409799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66622747HCID 66622747—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 66622302HCID 6662230295%

Reaction Steps

To a solution of crude [2-Benzyloxy-1-(2,2-dimethyl-[1,3]dioxolan-4-ylmethoxymethyl)-ethyl]-methyl-carbamic acid tert-butyl ester (1.25 g, 3.06 mmol) in MeOH (10 mL) was added Pd/C (300 mg). The mixture was transferred to an autoclave reactor, charged with 55 psi of hydrogen, and stirred. After 1.5 h, LCMS analysis indicated the completion of the reaction. The reaction mixture was then filtered through celite and concentrated under reduced pressure to give [1-(2,2-dimethyl-[1,3]dioxolan-4-ylmethoxymethyl)-2-hydroxy-ethyl]-methyl-carbamic acid tert-butyl ester (0.875 g, 95%), which was used without purification. LRMS (M−Boc+H+) m/z 220.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759374B2
Source datasetuspto-grants-2014_06
ORD IDord-b6925285c1db4478a418e6fb612d7ea3
Source noteuspto-grants-2014_06