참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 4-Decylaniline | HCID 92309 | — |
| 반응물 | Methyl 2-hydroxy-3-phenylbenzoate | HCID 241577 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(4-decylphenyl)-2-hydroxy-[1,1'-biphenyl]-3-carboxamide | HCID 23043616 | 90% |
반응 단계
To a tetrahydrofuran (20 ml) solution of 4-decylaniline (3.07 g, 13.14 mmol), cooled to 0°-5° C. (inert atmosphere), is added n-butyllithium (2.3 M, 13.14 mmol). The deeply colored solution is stirred for ten minutes, after which a tetrahydrofuran (20 ml) solution of methyl 3-phenylsalicylate (1.00 g, 4.38 mmol) is added. The temperature is allowed to rise to 25° C. over a 30 minute period. The reaction is quenched by pouring the contents into 10% hydrochloric acid (100 ml). The organics are extracted into ethyl acetate, washed with 10% hydrochloric acid, dried (sodium sulfate), and concentrated to give 2.77 g of crude solid. Chromatography (Kieselgel 60, dichloromethane) affords N-(4-decylphenyl)-2-hydroxy-[1,1'-biphenyl]-3-carboxamide (1.69 g, 90%), mp 74°-75° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04939133 |
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| 출처 데이터셋 | uspto-grants-1990_07 |
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| ORD ID | ord-1edfb796a5e84ba8bb90232aa25fb128 |
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| 출처 메모 | uspto-grants-1990_07 |
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