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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 390329생성일: 2026년 10월 25일

Hydrochloric Acid → 2-Amino-3-(4-fluorophenyl)propanenitrile hydrochloride

https://huagongshe.com/reaction/390329

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물2-(Diphenylmethyleneamino)-3-(4-fluorophenyl)propanenitrileHCID 58458910—
용매TetrahydrofuranHCID 8028—
생성물2-Amino-3-(4-fluorophenyl)propanenitrile hydrochlorideHCID 6711657793%

반응 단계

To a solution of 2-(diphenylmethyleneamino)-3-(4-fluorophenyl)propanenitrile (1.65 g, 5.02 mmol, 1.0 equiv) in THF (20.1 mL) was added HCl (5.53 mL of a 1 M aqueous solution, 5.53 mmol, 1.1 equiv). After stirring 3 h, the reaction was poured into water and washed with ether (×3). The aqueous layer was neutralized by the addition of 10 M NaOH and extracted with CH2Cl2 (×3). The combined CH2Cl2 extracts were dried (Na2SO4) and then concentrated in vacuo to provide the title compound (0.77 g, 93% yield) as a colorless oil. For convenience, the amine could be converted into the hydrochloride salt by dissolution in ether, treating with 2 M HCl in ether, and filtering the resulting white solid: 1H NMR (400 MHz, CDCl3) δ ppm 7.24-7.29 (m, 2H), 7.01-7.08 (m, 2H), 3.85-3.96 (m, 1H), 2.92-3.07 (m, 2H), 1.60 (d, J=7.55 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383639B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-efd309d3036c44b7be237f7d902e33b4
출처 메모uspto-grants-2013_02