참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Ethyl Acetoacetate | HCID 8868 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4-Methoxybenzyl bromide | HCID 165021 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | Ethyl 4-(4-Methoxybenzyl)acetoacetate | HCID 9992286 | — |
반응 단계
Into a 3 l. 3-necked r.b. flask equipped with a mechanical stirrer, thermometer, dropping funnel, and nitrogen gas inlet was placed 24 g. (0.5 mole) of 50% NaH prewashed with hexane, and 1000 ml. of dry tetrahydrofuran. 65 g. (0.5 mole) of ethyl acetoacetate was then added dropwise at -10° to 0° C. using a dry ice-acetone bath. After addition of ethyl acetoacetate was finished, the mixture was gradually warmed up to 10° C. in the course of 15 minutes and then 240 ml. (0.528 mole) of 2.2 M n-butyllithium was added dropwise maintaining temperature below -40° to -20° C. After the mixture was stirred at -10° for 15 minutes, 100.5 g. (0.5 mole) of 4-methoxybenzyl bromide was added dropwise over a period of 45 minutes at -10° C. The reaction mixture was gradually warmed up to room temperature and stirred for an additional hour, and then cooled to -20° C. 5 N HCl was then carefully added until the solution was slightly acidic.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04342692 |
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| 출처 데이터셋 | uspto-grants-1982_08 |
|---|
| ORD ID | ord-ebc5a886d01443d8abd527ad9465951c |
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| 출처 메모 | uspto-grants-1982_08 |
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