참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,1-Dichloroethane | HCID 6365 | — |
| 반응물 | 2-Octanone | HCID 8093 | — |
| 반응물 | 4-Iodoaniline | HCID 10893 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | N-(4'-iodophenyl)-2-aminooctane | HCID 9927521 | 88% |
반응 단계
A flask containing 4-iodoaniline (11.0 g, 50.2 retool) was charged with dry dichloroethane (125 ml), 2-octanone (7.9 ml, 50.0 retool) and sodium triacetexyborohydride (13.8 g, 65 retool). After stirring for 10 minutes, acetic acid (2.9 ml, 50.7 retool) was added via syringe over a 5 minute period. The reaction was stirred under an N2 atmosphere for 16 hrs. At the end of this period the reaction was quenched by the careful addition of a solution of saturated aqueous ammonium chloride (100 ml). After stirring for 0.5 hr, the reaction was poured over ether (250 ml) and the layers were separated. The ether layer was washed with saturated aqueous ammonium chloride (100 ml), dried (Na2SO4), filtered and evaporated in vacuo. Flash column chromatography (silica, 1:39; EtOAC:hexanes) provided N-(4'-iodophenyl)-2-aminooctane (14.6 g, 88%) as a light yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05424056 |
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| 출처 데이터셋 | uspto-grants-1995_06 |
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| ORD ID | ord-22213ec37f454f329b0a716ed24c074e |
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| 출처 메모 | uspto-grants-1995_06 |
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