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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2063719생성일: 2026년 10월 27일

Hydrochloric Acid → 1-Dimethylamino-4-[1-(1-ethoxy-ethoxy)-2-phenylethyl]cyclohexanecarbonitrile

https://huagongshe.com/reaction/2063719

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DimethylamineHCID 674—
반응물Potassium CyanideHCID 9032—
반응물4-[1-(1-Ethoxy-ethoxy)-2-phenylethyl]cyclohexanoneHCID 66887529—
용매MethanolHCID 887—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-Dimethylamino-4-[1-(1-ethoxy-ethoxy)-2-phenylethyl]cyclohexanecarbonitrileHCID 69810243—

반응 단계

40% aqueous dimethylamine solution (6.05 ml, 47.9 mmol) was added to a mixture of 4 M hydrochloric acid (2.61 ml) and methanol (1.56 ml), while cooling with ice. A solution of 4-[1-(1-ethoxy-ethoxy)-2-phenylethyl]cyclohexanone (2.91 g, 10.0 mmol) in methanol (6 ml) and tetrahydrofuran (3 ml) was added to this mixture. Thereafter, potassium cyanide (1.56 g, 24.1 mmol) was added to the mixture, the mixture was stirred at room temperature overnight, water (150 ml) was then added and the mixture was extracted with diethyl ether (4×50 ml). The combined organic phases were dried with sodium sulfate and concentrated i. vac. The residue was taken up in methylene chloride (50 ml) and the mixture was washed with water (30 ml). The organic phase was dried again with sodium sulfate and concentrated i. vac.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08288406B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-21c484039fc04503b1778d68549300f2
출처 메모uspto-grants-2012_10