Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethyl ketone → 4-((Benzyloxy)methyl)-2,2-diethyl-1,3-dioxolane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethyl ketone | HCID 7288 | — |
| 반응물 | 3-(Benzyloxy)-1,2-propanediol | HCID 98072 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-((Benzyloxy)methyl)-2,2-diethyl-1,3-dioxolane | HCID 59792527 | 67.1% |
반응 단계
To a tetrahydrofuran (30 ml) solution of DL-α-O-benzyl glycerol (3 g, 16.5 mmol), 3-pentanone (17.5 ml, 165 mmol) and p-toluenesulfonic acid monohydrate (300 mg, 1.58 mmol) were added at room temperature and the mixture was stirred at the same temperature for 22 hours. To the reaction mixture, a saturated aqueous sodium hydrogen carbonate solution (5 ml) was added to adjust pH to about 8. The generated precipitate was removed by filtration and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (NH silica gel, elution solvent: heptane/ethyl acetate=1/0 to 3/1 gradient). A desired fraction was concentrated to obtain the title compound (2.77 g, 67.1% yield) as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07425634B2 |
| 출처 데이터셋 | uspto-grants-2008_09 |
| ORD ID | ord-b0ba235f52084fb9baa50225f74f6979 |
| 출처 메모 | uspto-grants-2008_09 |