Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dimethyl terephthalate → Dimethyl Cyclohexane-1,1-dicarboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dimethyl terephthalate | HCID 8441 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 생성물 | Dimethyl Cyclohexane-1,1-dicarboxylate | HCID 10965525 | — |
반응 단계
In the past 1,4-CHDM has been made by a process in which dimethyl terephthalate is subjected to hydrogenation using a catalyst of Ru or Pd carried on alumina to give dimethyl cyclohexanedicarboxylate, and then a side chain of the resulting ester is subjected to a hydrogenation reaction in the presence of a Cu—Zn oxide catalyst, to manufacture 1,4-CHDM, as mentioned, for example, in JP-W-8-510686. In addition, in JP-A-6-228028 is described a process for the manufacture of 1,4-CHDM where dialkyl terephthalate is subjected to hydrogenation to give dimethyl 1,4-cyclohexanedicarboxylate, and then the side chain of the product is hydrogenated using a catalyst containing Ru and Sn to manufacture 1,4-CHDM.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06294703B1 |
| 출처 데이터셋 | uspto-grants-2001_09 |
| ORD ID | ord-40f343461978475187f66ce1d1919e8b |
| 출처 메모 | uspto-grants-2001_09 |