참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,4,5-Triphenylimidazole | HCID 10232 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Methyl 7-bromohept-5-ynoate | HCID 11287432 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 7-(1,2,4-Triphenyl-imidazolyl)-hept-5-ynoic acid | HCID 53688979 | — |
반응 단계
A solution of 2,4,5-triphenylimidazole (1.07 g) in dimethyl-formimide (20 ml) was treated with sodium hydride 50% in oil (0.17 g) and methyl 7-bromohept-5-ynoate (0.95 g). The solution was stirred for 18 hours when the solvent was removed under reduced pressure and the residue was chromatographed on silica gel eluted with chloroform hexane to give a clear oil which was dissolved in methanol (20 ml) and treated with 10% potassium hydroxide solution (10 ml) for 2 hours. The methanol was removed under reduced pressure and the remaining aqueous was acidified (pH 3) and filtered. The filtrate was extracted with chloroform (3×50 ml). The chloroform extracts were dried over magnesium sulphate, filtered and the solvent removed to give a solid which was recrystallised from acetonitrile to give 7-(1,2,4-triphenyl-imidazolyl)-hept-5-ynoic acid as white prisms, m.p. 144°-145° C.; Found: C, 79.99; H, 5.81; N, 6.40% (C28H24N2O2);Requires: C, 79.97; H, 5.75; N, 6.66%
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05663053 |
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| 출처 데이터셋 | uspto-grants-1997_09 |
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| ORD ID | ord-5267751af1ed4384aa2f4197c04d07a6 |
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| 출처 메모 | uspto-grants-1997_09 |
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