참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Tetrabutyltin | HCID 15098 | — |
| 반응물 | Tetradec-7-ene | HCID 25209 | — |
| 반응물 | CID 521661 | HCID 521661 | — |
| 촉매 | Tungsten hexachloride | HCID 83301 | — |
| 생성물 | Tetradec-7-ene | HCID 25209 | — |
| 생성물 | Hexadec-7-ene | HCID 520743 | — |
| 생성물 | CID 521661 | HCID 521661 | — |
반응 단계
7-Tetradecene and 9-octadecene were cross-metathesized employing a homogeneous modified catalyst. For the reaction, 1 mole 7-tetradecene and 1 mole 9-octadecene were combined in the reactor with 13 millimoles tungsten hexachloride. Triphenylphosphine (6.5 millimoles) was then charged to the reactor followed by the addition of 13 millimoles tetrabutyl tin. The reaction was conducted at 115° C and after 330 minutes reaction, near equilibrium conversion of the olefins was obtained with high selectivity to the equilibrium mixture of 1-part 7-tetradecene, 1 part 9-octadecene and 2 parts 7-hexadecene. When the experiment was repeated in an identical manner but using an unmodified catalyst (13 millimoles tungsten hexachloride with 13 millimoles tetrabutyl tin) conversion of the olefins was significantly greater than the theoretical equilibrium conversion due to the lower selectivity of the reaction to the desired cross-metathesized products.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04078012 |
|---|
| 출처 데이터셋 | uspto-grants-1978_03 |
|---|
| ORD ID | ord-fd439f1193024e988016522ffcf11a14 |
|---|
| 출처 메모 | uspto-grants-1978_03 |
|---|