Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hexamethylenetetramine → 4-(2-Phenylpropan-2-yl)benzaldehyde
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hexamethylenetetramine | HCID 4101 | — |
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Dimethyldiphenylmethane | HCID 13065 | — |
| 생성물 | 4-(2-Phenylpropan-2-yl)benzaldehyde | HCID 18509413 | 80.5% |
반응 단계
2,2-Diphenylpropane (3.93 g; 20.0 mmol) and hexamethylenetetramine (2.80 g; 20.0 mmol) were added to trifluoroacetic acid (35 ml), and the mixture was refluxed for 16 hours. The mixture was brought to room temperature, and poured into ice/water, followed by stirring for 1 hour. The pH of the mixture was adjusted to about 9 with potassium carbonate, followed by extraction with ether (100 ml). The organic layer was washed with saturated aqueous sodium bicarbonate solution, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=10:1), to thereby yield 3.61 g of the target compound (yield: 80.5%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06586633B1 |
| 출처 데이터셋 | uspto-grants-2003_07 |
| ORD ID | ord-171e9a76dd6b4c21b461fd0b5c16f2f9 |
| 출처 메모 | uspto-grants-2003_07 |