Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
O-Xylene → HCID 86737387, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | O-Xylene | HCID 7237 | — |
| 반응물 | 4-Piperidinol, 2,2,6,6-tetramethyl-1-(phenylmethyl)- | HCID 103602 | — |
| 반응물 | 1,2,2-Hexanetricarboxylic acid, triethyl ester | HCID 12296885 | — |
| 반응물 | HCID 178506930 | HCID 178506930 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | HCID 86737387 | HCID 86737387 | — |
반응 단계
30.2 g (0.1 mol) of triethyl hexane-1,2,2-tricarboxylate, 74.2 g (0.3 mol) of 1-benzyl-2,2,6,6-tetramethyl-4-hydroxypiperidine and 50 ml of xylene are warmed to 130° and mixed with 0.8 g of LiNH2. The ethanol formed is distilled off continuously. The solution is kept at the above temperature for 3 hours, so that it can then be kept at 150° for a further 2 hours. After cooling, the residue is taken up in toluene, a little glacial acetic acid is added to the solution and the latter is washed with H2O. After drying over Na2SO4, the solvent is distilled off in vacuo. Tris-(1-benzyl-2,2,6,6-tetramethyl-4-piperidinyl)hexane-1,2,2-tricarboxylate is obtained as a powdery residue. (Compound No. 1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04238613 |
| 출처 데이터셋 | uspto-grants-1980_12 |
| ORD ID | ord-f49222781930484c9ba96ee7d95aca35 |
| 출처 메모 | uspto-grants-1980_12 |