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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 580385생성일: 2026년 10월 25일

Iodoethane → HCID 15128680, 화합물

https://huagongshe.com/reaction/580385

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물DiisopropylamineHCID 7912—
반응물Lithium diisopropylamideHCID 2724682—
반응물HCID 14156194HCID 14156194—
반응물Carbontetrachloride dry-iceHCID 86602444—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
용매HexamethylphosphoramideHCID 12679—
생성물HCID 15128680HCID 15128680—

반응 조건

온도-78 °C

반응 단계

To a freshly prepared solution of lithium diisopropylamide in tetrahydrofuran (6 equivalents; prepared by addition of 19.2 ml of a 2.6M solution of n-butyllithium in hexane to 15 ml of freshly distilled diisopropylamine in 80 ml of tetrahydrofuran) at -78° C., was added 3.0 g (8.35 mmole) of 7-chloro-1,3,4,5-tetrahydro-3-(methoxycarbonyl)-4-(4-methoxyphenyl)-2H-1-benzazepin-2-one (see Example 1C . After stirring at -78° C. for 1.5 hours, 3 ml of hexamethylphosphoric triamide was added along with 13.6 ml of iodoethane (filtered through alumina to remove iodine). The mixture was stirred at -78° C. for 30 minutes (under argon), and then at -20° C. (dry-ice/carbon tetrachloride bath) for six days. The reaction was quenched with 1N hydrochloric acid (50 ml), and the aqueous layer was extracted with ethyl acetate (three times). The ethyl acetate extracts and the tetrahydrofuran were combined, washed with saturated sodium bicarbonate and saturated sodium chloride, and dried (magnesium sulfate). The solution was concentrated, combined with 0.31 g of previously prepared crude product and flash chromatographed (silica gel/3:1-hexane:ethyl acetate) yielding 0.61 g of product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04752645
출처 데이터셋uspto-grants-1988_06
ORD IDord-ef2f98eaa704433298f15a3ed1736cee
출처 메모uspto-grants-1988_06