Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869064Generated: October 30, 2026

Di-tert-butyl azodicarboxylate → HCID 89611118, compound

https://huagongshe.com/reaction/869064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant(2-Bromo-5-methoxypyridin-4-yl)boronic acidHCID 44119383—
CatalystCupric acetateHCID 8895—
SolventMethanolHCID 887—
ProductHCID 89611118HCID 8961111811.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2-bromo-5-methoxypyridine-4-boronic acid (10 g, 43.1 mmol), di-tert-butyl azodicarboxylate (9.93 g, 43.1 mmol), and copper(II) acetate (7.48 mg, 0.041 mmol) in MeOH (150 mL) was stirred 20 h at 50° C., filtered, concentrated, diluted with brine (100 mL), and extracted with EtOAc. The organic layers were combined, washed with brine, dried (Na2SO4), and concentrated. The residue was purified by silica gel column chromatography (hexane/EtOAc, 95:5→3:1) to provide 2.13 g of the title compound. tR: 1.21 min (LC-MS 4); ESI-MS: 418.2 [M+H]+ (LC-MS 4); Rf=0.67 (hexane/EtOAc, 1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969341B2
Source datasetuspto-grants-2015_03
ORD IDord-df590c170538427a9f77e7e09472edef
Source noteuspto-grants-2015_03