참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4-Mercaptophenol | HCID 240147 | — |
| 반응물 | 5-(Bromomethyl)-1,2,3-trimethoxybenzene | HCID 10355271 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-((3,4,5-Trimethoxybenzyl)thio)phenol | HCID 384136 | 68.7% |
반응 단계
4-Hydroxy thiophenol (12 g, 0.095 mol) and potassium carbonate (15.86 g, 0.115 mol) were dissolved in 250 ml of N,N-dimethylformamide, and cooled to 0° C. To the above solution at 0° C. was added dropwise 25 g (0.095 mol) of 3,4,5-trimethoxybenzyl bromide prepared in step (1) dissolved in 50 ml N,N-dimethylformamide. After stirring for 2 hr, the ice-bath was removed, and the solution was stirred overnight. The whole solution was poured into water, and extracted with 300 ml ethyl acetate. The organic layer was washed twice with 300 ml of water. Drying over magnesium sulfate, filtration, concentration, and chromatographic purification on silica gel column (ethyl acetate/n-hexane=2/3) gave 20 g (yield 68%) of 3,4,5-trimethoxybenzyl 4-hydroxyphenyl thioether as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05840991 |
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| 출처 데이터셋 | uspto-grants-1998_11 |
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| ORD ID | ord-577d302a667c416aaa4696872b29ad7f |
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| 출처 메모 | uspto-grants-1998_11 |
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