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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112091Generated: November 3, 2026

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

https://huagongshe.com/reaction/2112091

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
Reactant3-(Benzyloxy)cyclobutane-1-carboxylic acidHCID 12815111—
ReactantPhosphoric acid diphenylester azideHCID 66782931—
SolventDichloromethaneHCID 6344—
Producttert-Butyl [3-(benzyloxy)cyclobutyl]carbamateHCID 53415284—

Reaction Steps

9.28 g (45 mmol) 3-benzyloxy-cyclobutancarboxylic acid (Org. Lett. 6(11), 1853-1856, 2004) are suspended in 80 ml dry tert-butanol and combined with 5.1 g (50 mmol) triethylamine and 13.8 g (50 mmol) phosphoric acid diphenylester azide. The reaction mixture is stirred for 20 h under reflux conditions. The solvent is eliminated in vacuo and the residue is taken up in dichloromethane. The organic phase is washed three times with 2 N sodium hydroxide solution, dried with sodium sulphate and the dichloromethane is eliminated in vacuo. The crude product is recrystallised from acetonitrile (1 g crude product: 5 ml acetonitrile).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521457B2
Source datasetuspto-grants-2009_04
ORD IDord-87a78f87589549f787aa886342058bac
Source noteuspto-grants-2009_04