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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340937Generated: October 31, 2026

HCID 66622747, compound → HCID 66622302, compound

https://huagongshe.com/reaction/340937

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 numberUS08895582B2
Source datasetuspto-grants-2014_11
ORD IDord-cd336df3c1184ca48e51bc6b44b738fe
Source noteuspto-grants-2014_11