Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754285Generated: November 1, 2026

HCID 118222064, compound → 3-Azabicyclo[5.1.0]octan-5-ol

https://huagongshe.com/reaction/1754285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 118222064HCID 118222064—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-Azabicyclo[5.1.0]octan-5-olHCID 11822206369.11%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of benzyl 3-hydroxy-5-azabicyclo[5.1.0]octane-5-carboxylate (110.00 mg, 420.94 umol, 1.00 Eq) in MeOH (10 mL) was added Pd—C under N2. The suspension was degassed under vacuum and purged with H2 several times. The mixture was stirred under H2 at 25° C. for 4 hr. TLC showed the starting material was consumed completely. The reaction mixture was filtered and the filter was concentrated to give 5-azabicyclo[5.1.0]octan-3-ol (37.00 mg, 290.93 umol, 69.11% yield) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169212B2
Source datasetuspto-grants-2015_10
ORD IDord-bcb1fa9392d947dbb1cbc3f93c0e9fa1
Source noteuspto-grants-2015_10