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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730027Generated: October 30, 2026

N,N,N',N'-Tetramethylazodicarboxamide → HCID 68814169, compound

https://huagongshe.com/reaction/730027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylazodicarboxamideHCID 4278—
ReactantPhthalimideHCID 6809—
ReactantTributylphosphineHCID 13831—
ReactantHCID 68814812HCID 68814812—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68814169HCID 68814169—

Reaction Steps

The crude 1-(azulen-1-yl)ethanol prepared in Example 72, Step A was dissolved in dehydrated THF (380 mL), and stirred with cooling on ice under nitrogen atmosphere. This reaction mixture was added with phthalimide (45.0 g, Kanto Kagaku), tri-n-butylphosphine (37.7 mL, Kanto Kagaku), and 1,1′-azobis(N,N′-dimethylformamide) (26.3 g, Midori Kagaku), and stirred at room temperature for 16 hours under nitrogen atmosphere. The solid was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was added with saturated aqueous sodium hydrogencarbonate, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate=6:1), to obtain 16.8 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582658B2
Source datasetuspto-grants-2009_09
ORD IDord-4ab183ad67194a0c9753cf73d6050c4f
Source noteuspto-grants-2009_09