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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylazodicarboxamide | HCID 4278 | — |
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | HCID 68814812 | HCID 68814812 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68814169 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582658B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-4ab183ad67194a0c9753cf73d6050c4f |
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| Source note | uspto-grants-2009_09 |
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