참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Decanol | HCID 8174 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| 반응물 | (6-Hydroxy-2-naphthyl)-propanonitrile | HCID 19097091 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (6-n-Decyloxy-2-naphthyl)propanonitrile | HCID 67849695 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05160662 |
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| 출처 데이터셋 | uspto-grants-1992_11 |
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| ORD ID | ord-842523f6f5274584a748f187a6a500e1 |
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| 출처 메모 | uspto-grants-1992_11 |
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