Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Cyclohexylamine → N-cyclohexyladamantane-1-carboxamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Cyclohexylamine | HCID 7965 | — |
| 반응물 | 1-Adamantanecarboxylic acid | HCID 13235 | — |
| 반응물 | N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamine | HCID 136149 | — |
| 생성물 | N-cyclohexyladamantane-1-carboxamide | HCID 3452412 | — |
반응 단계
1-Adamantanecarboxylic acid (10.8 g, 0.06 mole) was dissolved in N,N-diethyl-1,1,2,3,3,3-hexafluoropropylamine (13.4 g, 0.06 mole) as described in example 1. After the reaction mixture cooled to room temperature, cyclohexylamine (14.88 g, 17.2 ml, 0.15 mole) was added slowly and a heavy precipitate of the amide appeared almost immediately. The N-cyclohexyl-1-adamantanecarboxamide was isolated as described in example 1 to give 14.8 g, 94.4%; mp 199.3-200.4° C. The analytical sample was recrystallized from cyclohexane and sublimed. Anal. Calcd. for C17H27NO: C, 78.18; H. 10.34; N, 5.36. Found: C, 77.97; H, 10.46; N, 5.32.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06348625B1 |
| 출처 데이터셋 | uspto-grants-2002_02 |
| ORD ID | ord-1c6b89b49b8d4241b5311b90b3e12366 |
| 출처 메모 | uspto-grants-2002_02 |