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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1383007생성일: 2026년 10월 26일

Hydrochloric Acid → HCID 14372069, 화합물

https://huagongshe.com/reaction/1383007

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2,2,6,6-TetramethylpiperidineHCID 13035—
반응물DimethylaminopropionitrileHCID 15615—
반응물N,N-diethyl-2-methylfuran-3-carboxamideHCID 4694183—
반응물ButyllithiumHCID 178418339—
용매AcetoneHCID 180—
용매TetrahydrofuranHCID 8028—
생성물HCID 14372069HCID 1437206982%

반응 단계

To a solution of 2,2,6,6-tetramethylpiperidine (5.1 ml, 30.4 mmole) in dry tetrahydrofuran (60 ml), cooled at -78° C. (dryice/acetone) under an argon atmosphere, was added dropwise n-butyllithium (17.3 ml, 27.6 mmole). After the addition the reaction was warmed to -10° C. (ice/acetone). To this solution was added N,N-diethyl-2-methylfuran-3-carboxamide (5.0 g, 27.6 mmole) in tetrahydrofuran (15 ml). After stirring this mixture for 1.0 hour, 3-(dimethylamino)propionitrile (3.27 ml, 29.0 mmole) was added dropwise. The reaction was allowed to warm overnight. The reaction was poured into ice/water and acidified to a pH 3.25 with hydrochloric acid. The mixture was then extracted with diethyl ether (3×150 ml). The pH of the aqueous layer was adjusted to 13.0 using sodium hydroxide solution (40%) and this solution was extracted exhaustively using methylene chloride (10×150 ml). The combined extracts were washed with water (2×50 ml), brine (2×100 ml) and dried (MgSO4). After solvent evaporation 8.25 g of an oil was obtained. This was purified by flash chromatography using 15% methanol/chloroform as the eluting solvent to give analytically pure product (4.65 g, 82% yield), mp: 97.5°-98.0° C. Some starting amide (1.05 g) was recovered from the initial diethyl ether extracts.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04808595
출처 데이터셋uspto-grants-1989_02
ORD IDord-91f6b64d6f0c48329c9d5d22b8cb6f8a
출처 메모uspto-grants-1989_02