HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169212Generated: November 1, 2026
1-Naphthaleneacetonitrile → HCID 13980433, compound
https://huagongshe.com/reaction/2169212
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Naphthaleneacetonitrile | HCID 8596 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13980433 | HCID 13980433 | 91% |
Reaction Steps
To a stirred suspension of NH4Cl (1.6 g, 30 mmol) in anhydrous toluene (50 mL) was added trimethyl aluminium (2M in toluene, 15 mL, 30 mmol) at 0° C. The mixture was then warmed to room temperature and stirred for 2 h. A solution of 2-(naphthalen-1-yl)acetonitrile (1.67 g, 10 mmol) in toluene (10 mL) was added to the above reaction mixture and the reaction mixture was stirred at 80° C. for 18 h. After completion of the reaction, the reaction mixture was quenched with a suspension of silica gel in chloroform. The mixture was stirred at room temperature for 0.5 h before being filtered through a sintered funnel. The silica gel was washed with methanol. The combined filtrate was concentrated under reduced pressure to give the crude product as an off-white solid (2 g, 91%), which was used directly without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045486B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-51a1a775da9c4588a6853e16b34ffd23 |
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| Source note | uspto-grants-2015_06 |
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