HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372928Generated: October 25, 2026
1-Decanol → (6-n-Decyloxy-2-naphthyl)propanonitrile
https://huagongshe.com/reaction/372928
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Decanol | HCID 8174 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (6-Hydroxy-2-naphthyl)-propanonitrile | HCID 19097091 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-n-Decyloxy-2-naphthyl)propanonitrile | HCID 67849695 | — |
Reaction Steps
Into 20 ml of dry THF, were dissolved 1.5 g of oa (6-hydroxy-2-naphthyl)-propanonitrile and 3.0 g of triphenylphosphine, and cooled to 5° C. To this solution, were added dropwise 2.0 g of diethyl azodicarboxylate and then 1.2 g of n-decyl alcohol, and stirred at room temperature for 12 hours. The resulting reaction mixture was extracted with ether, followed by washing three times the ether phase with water and then distilling off the ether. The resulting oily product was extracted with hexane, and the hexanesoluble matter was recrystallized with methanol to obtain 0.7 g of oa (6-n-decyloxy-2-naphthyl)propanonitrile (Compound No. 1-10) of this invention.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05160662 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-842523f6f5274584a748f187a6a500e1 |
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| Source note | uspto-grants-1992_11 |
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