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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

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물TetrahydrofuranHCID 8028—
반응물Ethyl 7-bromoheptanoateHCID 122490—
반응물1-Ethoxyethyl etherHCID 10464631—
반응물ButyllithiumHCID 178418339—
용매HexaneHCID 8058—
용매HexamethylphosphoramideHCID 12679—
생성물alpha-(6-Carbethoxyhexyl)-alpha-(1-ethoxyethoxy)-alpha-(2-furyl)acetonitrileHCID 20366327—

반응 조건

온도-5 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04076732
출처 데이터셋uspto-grants-1978_02
ORD IDord-d13e41016c574999a01beb05ec7ae6c6
출처 메모uspto-grants-1978_02