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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454791Generated: October 29, 2026

Dimethylformamide → Azide

https://huagongshe.com/reaction/454791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPentamethyldiethylenetriamineHCID 18196—
Reactant2-Bromo-2-methylpropionyl bromideHCID 88685—
ReactantAzide propanolHCID 86658298—
SolventTetrahydrofuranHCID 8028—
ProductAzideHCID 33558—
Productalpha-BromoisobutyrateHCID 6993926—

Reaction Steps

An azide functionalized ATRP initiator (azidepropyl 2-bromoisobutyrate, AzPBIB) was prepared by the esterification reaction of azide propanol with α-bromoisobutyryl bromide in anhydrous THF at 0° C. for overnight. AzPBIB was then introduced to alkyne-functionalized PEG copolymer via click chemistry. In a typical procedure, poly(OEGMA-co-PgTEGMA) (0.1 g, 0.09 mmol based on alkyne groups), AzPBIB (9.2 mg, 0.037 mmol), CuBr (5.3 mg, 0.037 mmol), PMDETA (6.4 mg, 0.037 mmol) and DMF (0.5 mL) were added to a Schlenk tube. The reaction tube was degassed by three freeze-pump-thaw cycles, sealed under vacuum, and placed in a 40° C. oil bath for 24 h. After cooling to room temperature, the flask was exposed to air. After removing most of the solvents at reduced pressure, the residues were dissolved in DCM and passed through a neutral alumina column to remove copper catalysts. The solution was then concentrated under reduced pressure and precipitated in hexane. The isolated polymer poly(OEGMA-co-PgTEGMA-co-BIBTEGMA) was dried under vacuum. The bromoisobutyrate ratio in the final copolymer is approximately 12% as determined by 1H NMR analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08496997B2
Source datasetuspto-grants-2013_07
ORD IDord-6a1454b262f2442abe0a2b8dbb691a17
Source noteuspto-grants-2013_07