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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162909Generated: October 28, 2026

N,N,N',N'-Tetramethylazodicarboxamide → 2-[2-(2-Benzyloxyethoxy)ethoxy]benzonitrile

https://huagongshe.com/reaction/1162909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylazodicarboxamideHCID 4278—
Reactant2-HydroxybenzonitrileHCID 11907—
ReactantTributylphosphineHCID 13831—
Reactant2-[2-(Benzyloxy)ethoxy]ethan-1-olHCID 229722—
SolventTolueneHCID 1140—
Product2-[2-(2-Benzyloxyethoxy)ethoxy]benzonitrileHCID 5755807771%

Reaction Steps

2-Hydroxybenzonitrile (300 mg, 2.52 mmol), di(ethylene glycol) benzyl ether (593 mg, 3.02 mmol), and 1,1′-azobis(N,N-dimethylformamide) (867 mg, 5.04 mmol) were dissolved in toluene (15 ml). Thereafter, tri-n-butylphosphine (1.26 ml, 5.04 mmol) was added at 20° C. to the obtained solution, and the obtained mixture was stirred at the same above temperature for 2 hours. The generated precipitate was filtrated, and the filtrate was then diluted with ethyl acetate (20 ml). The ethyl acetate solution was washed with water twice, and then with a saturated saline solution once. The resultant was dried over anhydrous sodium sulfate, and was then concentrated under reduced pressure. The obtained pale brown oil product was purified by silica gel column chromatography (dichloromethane), so as to obtain 2-[2-(2-benzyloxyethoxy)ethoxy]benzonitrile (529 mg, 71%) in the form of a colorless oil product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820693B2
Source datasetuspto-grants-2010_10
ORD IDord-2f61d2458c2e40978e99b1bfd18fbc5a
Source noteuspto-grants-2010_10