참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzene | HCID 241 | — |
| 반응물 | Potassium phosphate sodium hydroxide | HCID 86597010 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 반응물 | HCID 178506046 | HCID 178506046 | — |
| 용매 | Cyclohexane | HCID 8078 | — |
| 생성물 | Cyclohexanol | HCID 7966 | — |
| 생성물 | Cyclohexene | HCID 8079 | — |
반응 단계
In a high pressure glass bomb (ca. 20 ml), 200 mg. of the catalyst prepared above, 2 ml. of benzene, and 5 ml. of 40% sulfuric acid were provided with a small bar magnet coated with polytetrafluoroethylene. After replacement with hydrogen, the bomb was heated at 100° C. under 10 Kg/cm2G pressure of hydrogen for 4 hours with magnetic stirring. After neutralization with about 13 ml. of aqueous alkali (ca. 40%K3PO4 -NaOH), the product was submitted to gas-liquid chromatography (column: 25%PEG-4000/C-22, 60-80 mesh, 3 m., 150° C., H2 20 ml./min). The chromatogram showed that the conversion of benzene was 1.39%, and the yields of cyclohexanol, cyclohexane, and cyclohexene were 0.42%, 0.77%, and 0.20%, respectively. The selectivity of cyclohexanol was 30%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04212990 |
|---|
| 출처 데이터셋 | uspto-grants-1980_07 |
|---|
| ORD ID | ord-e22c4d1cea9c40b0aff009a9c8f3d8af |
|---|
| 출처 메모 | uspto-grants-1980_07 |
|---|