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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112092Generated: October 30, 2026

tert-Butyl [3-(benzyloxy)cyclobutyl]carbamate → tert-Butyl (3-hydroxycyclobutyl)carbamate

https://huagongshe.com/reaction/2112092

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl [3-(benzyloxy)cyclobutyl]carbamateHCID 53415284—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Producttert-Butyl (3-hydroxycyclobutyl)carbamateHCID 22594430—

Reaction Conditions

Temperature45 °C

Reaction Steps

2.77 g (10 mmol) tert.butyl (3-benzyloxy-cyclobutyl)-carbamate are suspended in 100 ml of methanol and combined with 200 mg palladium hydroxide. The reaction mixture is stirred for 5 h at 45° C. and 45 bar H2 pressure. Then the catalyst is filtered off and the solvent is eliminated in vacuo. The residue is taken up in chloroform and washed three times with aqueous sodium hydrogen carbonate solution. The organic phase is dried with magnesium sulphate and the solvent is eliminated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521457B2
Source datasetuspto-grants-2009_04
ORD IDord-2ce3e629d74f48249c2bb4dd59c50ac9
Source noteuspto-grants-2009_04