참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 5-Chloro-salicylaldehyde | HCID 12481 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 1,4-Dichloro-2-butene, (2E)- | HCID 642197 | — |
| 반응물 | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5-Chloro-2-(4-chloro-trans-2-butenyloxy)-benzaldehyde | HCID 15572712 | — |
반응 단계
To 1.2 lt of refluxing water, 1 ml of 40% aqueous tetrabutylammonium hydroxide, 160 g of 5-chloro-salicylaldehyde and 140 ml of trans-1,4-dichloro-2-butene are added while vigorously stirring, followed by the dropwise addition of the solution of 42 g of sodium hydroxide in 200 ml of water at such a rate that the pH of the mixture is kept between 7 and 8. Thereafter the mixture is refluxed until the pH is about 7, cooled and extracted with methylene chloride. The extract is washed with 5% aqueous sodium hydroxide, dried, evaporated and the residue heated to 30°/0.1 mmHg in order to remove the excess of 1,4-dichloro-2-butene. The residue is taken up in 1 lt of diethyl ether, the solution filtered, the filtrate evaporated and the residue recrystallized from ethyl acetate, to yield the 5-chloro-2-(4-chloro-trans-2-butenyloxy)-benzaldehyde melting at 62°-63°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04261907 |
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| 출처 데이터셋 | uspto-grants-1981_04 |
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| ORD ID | ord-90bd1998b87d471981ccc0612f614506 |
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| 출처 메모 | uspto-grants-1981_04 |
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