참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | 4-Azidomethyl-2'-cyanobiphenyl | HCID 10353989 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-[4-(Aminomethyl)phenyl]benzonitrile | HCID 1393341 | — |
반응 단계
A solution of 4-azidomethyl-2'-cyanobiphenyl (4.68 g, 20 mmole) in 40 ml of dry tetrahydrofuran (THF) was stirred under N2 at room temperature as 5.3 g (20 mmole) of triphenylphosphine was added in small portions over a period of about 10 minutes. After 2 hours, by which time gas evolution had ceased, 532 μl (532 mg, 29.6 mmole) of H2O was added. After an additional 23 hours, the solution was concentrated in vacuo to give a pale golden gum. This material was chromatographed on a column of silica gel (50×8.5 cm) packed in CH2Cl2. The column was eluted with a gradient of 0-6% methanol in CH2Cl2. Concentration of the product fractions gave a foam which solidified upon trituration with ether. This material was collected on a filter, washed further with some ether, and dried in vacuo at 50° C. to give white crystals, of satisfactory purity; mass spectrum (FAB) m/e 209 (M+1)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05281614 |
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| 출처 데이터셋 | uspto-grants-1994_01 |
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| ORD ID | ord-481edb139da147e6bc2ccf89d6aca787 |
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| 출처 메모 | uspto-grants-1994_01 |
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