Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 616851생성일: 2026년 10월 27일
Diisopropylamine → alpha-(6-Carbethoxyhexyl)-alpha-(1-ethoxyethoxy)-alpha-(2-furyl)acetonitrile
https://huagongshe.com/reaction/616851
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Ethyl 7-bromoheptanoate | HCID 122490 | — |
| 반응물 | 1-Ethoxyethyl ether | HCID 10464631 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Hexane | HCID 8058 | — |
| 용매 | Hexamethylphosphoramide | HCID 12679 | — |
| 생성물 | alpha-(6-Carbethoxyhexyl)-alpha-(1-ethoxyethoxy)-alpha-(2-furyl)acetonitrile | HCID 20366327 | — |
반응 단계
To a stirred solution of 84 ml of diisopropylamine in 280 ml of dry tetrahydrofuran (THF) is added 260 ml of 2.3M n-butyllithium in hexane during 30 min. at 0°-5° C. After stirring for 25 min. at -5° C. the solution is cooled to -75° C. and treated with a solution of 113g (0.58 mol) of 1-ethoxyethyl ether of furfural cyanohydrin (Example 1) in 115 ml of hexamethylphosphoric triamide during 45 min. at -75° to -65° C. After stirring for 25 min. at -75° C. the solution is treated with 136g (0.576 mol) of ethyl 7-bromoheptanoate during 40 min. -75° to -65° C. After slow addition of 280 ml of TMF as rinse the mixture is stirred at -75° C. for 2.5 hr. and at ambient temperature for 18 hr. The reaction mixture is partitioned with water and ether. The ether phase is washed with brine, dried over sodium sulfate, filtered through Celite, and concentrated.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04076732 |
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| 출처 데이터셋 | uspto-grants-1978_02 |
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| ORD ID | ord-d13e41016c574999a01beb05ec7ae6c6 |
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| 출처 메모 | uspto-grants-1978_02 |
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