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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891690Generated: October 30, 2026

1-Benzyloxycarbonyl-3-t-butyldiphenylsilyloxyazetidine → 3-((Tert-butyldiphenylsilyl)oxy)azetidine

https://huagongshe.com/reaction/891690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyloxycarbonyl-3-t-butyldiphenylsilyloxyazetidineHCID 22242980—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-((Tert-butyldiphenylsilyl)oxy)azetidineHCID 1784253196%

Reaction Steps

A solution of 1-benzyloxycarbonyl-3-t-butyldiphenylsilyloxyazetidine (4.04 g, 9.07 mmol) in methanol (200 ml) was subjected to catalytic hydrogenation in the presence of 10% palladium on charcoal (4.04 g) at room temperature for 1.5 hours. After checking the completion of the reaction, the reaction mixture was filtered and the filtrate concentrated under reduced pressure, and the obtained residue was dried under reduced pressure to give 3-t-butyldiphenylsilyloxyazetidine (2.70 g, yield 96%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-ceb202c0d7184921b257f679182172b6
Source noteuspto-grants-2006_02