Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetone → 4-[(4-Bromophenoxy)methyl]-2,2,4-trimethyl-1,3-dioxolane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetone | HCID 180 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 3-(4-Bromophenoxy)-2-methylpropane-1,2-diol | HCID 71059322 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 4-[(4-Bromophenoxy)methyl]-2,2,4-trimethyl-1,3-dioxolane | HCID 71059331 | 40.2% |
반응 단계
3-(4-Bromophenoxy)-2-methylpropane-1,2-diol (261 mg, 1.00 mmol), acetone (77 mg, 1.3 mmol), tetrahydrofuran (5 mL), and a boron trifluoride diethyl ether complex (3 drops) were mixed. The mixture was stirred at room temperature for 67 hours, and acetone (102 mg, 1.76 mmol) was added thereto, followed by stirring for 2 hours. Sodium carbonate, ethyl acetate, and water were added to the reaction mixture to conduct extraction. The organic layer was washed with a saline solution twice. A residue was obtained by concentrating the organic layer under reduced pressure, and the residue was subjected to chromatography refining (methylene chloride) using silica gel, obtaining 121 mg of the objective compound (yield: 40%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08598358B2 |
| 출처 데이터셋 | uspto-grants-2013_12 |
| ORD ID | ord-771e027b372243a5a31bf786fb682a8a |
| 출처 메모 | uspto-grants-2013_12 |