참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl cyanoformate | HCID 69336 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | ethyl [1-(toluene-4-sulfonyl)-1H-imidazol-4-yl]-acetate | HCID 86623936 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Diethyl 2-[1-(toluene-4-sulfonyl)-1H-imidazol-4-yl]malonate | HCID 67443784 | 32% |
반응 단계
A solution of 1.000 g (3.243 mmol) of ethyl [1-(toluene-4-sulfonyl)-1H-imidazol-4-yl]-acetate was dissolved in 20 ml of THF and cooled to 0° C. Over a period of 10 min, 3.567 ml of lithium bis(trimethylsilyl)amide (3.567 mmol, 1M in THF) were added dropwise. This mixture was stirred at 0° C. for 30 min, 350 μl (3.567 mmol) of ethyl cyanoformate were then added and the mixture was stirred at RT for another 2 h. The reaction mixture was quenched with saturated ammonium chloride solution and extracted with ethyl acetate. The organic phase was washed with water and saturated NaCl solution, dried over Na2SO4, filtered and concentrated. Chromatography on silica gel (heptane/ethyl acetate 1:1) gave the title compound (0.390 g, 32%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08044208B2 |
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| 출처 데이터셋 | uspto-grants-2011_10 |
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| ORD ID | ord-41dda38ecaf3417a8701b38aed097dfe |
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| 출처 메모 | uspto-grants-2011_10 |
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