참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N,N'-Diphenyl-P-Phenylenediamine | HCID 6319 | — |
| 반응물 | (+-)-alpha-Pinene | HCID 6654 | — |
| 반응물 | 3-Iodotoluene | HCID 12268 | — |
| 반응물 | sodium 2-methylpropan-2-olate | HCID 178418730 | — |
| 촉매 | Cuprous chloride | HCID 62652 | — |
| 촉매 | 2-(5,6-Diphenyl-2-pyridyl)pyridine | HCID 9861424 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | N,N'-Diphenyl-N,N'-di(m-tolyl)-1,4-phenylenediamine | HCID 14250518 | 90.5% |
반응 단계
A mixture of 31.2 g (0.12 mole) of N,N′-diphenyl-N,N′-p-phenylenediamine, 54.5 g (0.25 mole) of m-iodotoluene, 32.6 g (0.34 mole) of t-butoxy sodium, 59.0 mg (0.6 mmole) of copper (I) chloride, 185 mg (0.6 mmole) of 2-(5,6-diphenyl-2-pyridyl)pyridine (A-8) and 87.6 ml of α-pinene was reacted at 125 to 130° C. for 5 hours under a nitrogen gas stream. After completion of the reaction, 66 ml of toluene and 66 ml of water were added to separate the reaction mixture. Toluene was then concentrated under reduced pressure. The residue was crystallized by the addition of 39 ml of ethyl acetate and 253 ml of isopropanol, whereby 47.8 g (yield: 90.5%) of the target compound was obtained as pale yellow crude crystals. The compound was found to have a melting point of 170 to 171° C. and an HPLC content (column: YMC-A-002, UV detector: 310 nm, eluent having a flow rate of 1.1 ml/min) was 99.5%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06603007B1 |
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| 출처 데이터셋 | uspto-grants-2003_08 |
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| ORD ID | ord-ec820f4221474c6e9e960e66d32ab375 |
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| 출처 메모 | uspto-grants-2003_08 |
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