Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pentamethylbenzene → 5,7-di-tert-butyl-3-(2,3,4,5,6-pentamethylphenyl)-3H-benzofuran-2-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pentamethylbenzene | HCID 12784 | — |
| 반응물 | Tin tetrachloride | HCID 24287 | — |
| 반응물 | 5,7-Di-tert-butyl-3-hydroxy-2-benzofuranone | HCID 6850821 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5,7-di-tert-butyl-3-(2,3,4,5,6-pentamethylphenyl)-3H-benzofuran-2-one | HCID 10916196 | 89.3% |
반응 단계
11.5 g (77.5 mmol) of pentamethylbenzene and 10 ml (85.0 mmol) of tin tetrachloride are added to a solution of 19.7 g (75.0 mmol) of 5,7-di-tert-butyl-3-hydroxy-3H-benzofuran-2-one (compound (201), Table 2, Example 1a) in 50 ml of 1,2-dichloroethane and the reaction mixture is refluxed for 1 hour. The reaction mixture is diluted with water and extracted three times with toluene. The organic phases are combined, washed with water, dried over sodium sulfate and concentrated on a vacuum rotary evaporator. Crystallisation of the residue from ethanol yields 26.3 g (89%) of 5,7-di-tert-butyl-3-(2,3,4,5,6-pentamethylphenyl)-3H-benzofuran-2-one, m.p. 185°-190° C. (compound (111), Table 1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05814692 |
| 출처 데이터셋 | uspto-grants-1998_09 |
| ORD ID | ord-b321d29d51a34e9698917de377eb8ef9 |
| 출처 메모 | uspto-grants-1998_09 |