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HRID 2110628생성일: 2026년 10월 27일

Hydrochloric Acid → 2-[4-(Trifluoromethoxy)phenyl]ethan-1-amine hydrochloride

https://huagongshe.com/reaction/2110628

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Trifluoromethoxy-(2-nitro-vinyl)-benzeneHCID 688233—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물2-[4-(Trifluoromethoxy)phenyl]ethan-1-amine hydrochlorideHCID 4294208957%

반응 단계

A solution of 4-trifluoromethoxy benzaldehyde (1 g, 5.26 mmol) and nitromethane (0.96 g, 15.8 mmol) in acetic acid (10.6 mL) is treated with ammonium acetate (1.01 g, 13.2 mmol) is heated under microwave to 150° C. for 15 minutes. The reaction mixture is diluted with water, and extracted three times with DCM (50 mL). The combined extracts are washed sequentially with 2 N sodium hydroxide, water, and brine, dried over sodium sulfate and concentrated. The residue is subjected to silica gel chromatography to yield 4-trifluoromethoxy-(2-nitro-vinyl)-benzene (1.23 g) as a solid. A portion of 4-trifluoromethoxy-(2-nitro-vinyl)-benzene (0.504 g, 2.16 mmol) is hydrogenated with hydrogen in a balloon, 10% Pd/C (115 mg, 5 mol %) in MeOH (22 mL) containing concentrated hydrochloric acid (0.27 mL) at room temperature for 15 hours. The mixture is filtered and filtrate is concentrated to a solid that is washed with diethyl ether to obtain 2-(4-trifluoromethoxy-phenyl)-ethylamine hydrochloride [0.3 g, 57%, Intermediate (12)] as a solid. LC/MS: MS: 206 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07517889B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-de8d9d61dfa7453b823e26836705c805
출처 메모uspto-grants-2009_04