참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dopac | HCID 547 | — |
| 반응물 | Vinyl Acetate | HCID 7904 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 촉매 | Mercuric oxide | HCID 30856 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 5-(2-Hydroxyethyl)-2-methyl-1,3-benzodioxole | HCID 19001625 | 74.6% |
반응 단계
A suspension of 1.0 g of 3,4-dihydroxyphenylacetic acid, 1.4 g of vinyl acetate, 6 mg of mercury oxide (yellow) and 0.03 ml of boron fluoride/ethyl etherate in 9 ml of toluene was stirred at room temperature for 14 h. The reaction mixture was diluted with ethyl acetate and washed with water and an aqueous common salt solution. The organic layer was dried over magnesium sulfate and the solvent was distilled off. An oil thus obtained was dissolved in 10 ml of tetrahydrofuran and the solution was added dropwise to a suspension of 0.5 g of lithium aluminum hydride in tetrahydrofuran under cooling with ice. The mixture was stirred at room temperature for 1 h. 0.5 ml of water, then 0.5 ml of a 15% aqueous sodium hydroxide solution and finally 1.5 ml of water were added thereto and an insoluble matter was filtered off. The filtrate was concentrated and treated according to silica gel column chromatography (ethyl acetate/hexane=1:1) to obtain 0.8 g of the intended compound in the form of a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05475024 |
|---|
| 출처 데이터셋 | uspto-grants-1995_12 |
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| ORD ID | ord-237408a16d374957be2a2740e478e8d8 |
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| 출처 메모 | uspto-grants-1995_12 |
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