참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | 3-Chloro-1-propanol | HCID 12313 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 1-(4-Hydroxyphenyl)-3-phenylprop-2-en-1-one | HCID 94240 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-(3-Hydroxypropyloxy)-chalcone | HCID 68472192 | — |
반응 단계
A refined 4′-(3-hydroxypropyloxy)-chalcone (9.71 g, 34.4 mmol) was obtained with a yield of 51.4% by adding 90 ml of dry DMF to 4′-hydroxychalcone (15.0 g, 67 mmol) in an air current of argon, and adding sodium hydride (60%, 2.68 g, 67 mmol) through dropping in a reaction flask of 200 ml in ice cooling for 30 minutes; later, after heating to a room temperature and stirring for 5 hours, adding 3-chloro-1-propanol (6.33 g, 67 mmol) through dropping at the same temperature for 10 minutes; furthermore, heating to 80° C., and reacting for 7 hours; next, after injecting the solution into water with ice and extracting the product with ethyl acetate, washing with water, and drying through dehydration with magnesium sulfate, and removing the solvent; after refining (mobile phase, hexane:ethyl acetate=4:1) the gained coarse crystal with silica gel column, recrystallizing with ethyl acetate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06495221B1 |
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| 출처 데이터셋 | uspto-grants-2002_12 |
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| ORD ID | ord-6313d0c580d9494795cb6dc933f0fa1b |
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| 출처 메모 | uspto-grants-2002_12 |
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