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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104129Generated: October 30, 2026

Sodium Azide → tert-Butyl [1-(4-bromophenyl)cyclobutyl]carbamate

https://huagongshe.com/reaction/2104129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(4-Bromophenyl)cyclobutane-1-carboxylic acidHCID 16769919—
CatalystTetrabutylammonium BromideHCID 74236—
CatalystZinc trifluoromethanesulfonateHCID 104671—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl [1-(4-bromophenyl)cyclobutyl]carbamateHCID 52988051—

Reaction Steps

1-(4-bromophenyl)cyclobutanecarboxylic acid (7-1, 10.89 g, 42.7 mmol), Boc anhydride (10.90 mL, 47.0 mmol), sodium azide (9.71 g, 149 mmol), tetrabutylammonium bromide (2.048 mL, 6.40 mmol) and zinc trifluoromethansulfonate (0.155 g, 0.427 mmol) were stirred in THF (100 ml) at 60° for 4 h. The reaction mixture was cooled to room temperature and EtOAc and saturated aqueous sodium bicarbonate were added to the mixture. The suspension was filtered through a glass frit and the filtrate was extracted with EtOAc, washing with water and brine. The organic layer was dried over Na2SO4, filtered and reduced in vacuo to a tan oil. The crude product was purified by normal phase flash chromatography eluting with 5-15% EtOAc/Hex to give 7-2 as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576209B2
Source datasetuspto-grants-2009_08
ORD IDord-b8c2819607184ac69034d983164d0dee
Source noteuspto-grants-2009_08