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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1094368생성일: 2026년 10월 26일

Triethylamine → 2-Bromo-N-(3,4-dimethyl-phenyl)-N-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-acetamide

https://huagongshe.com/reaction/1094368

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Bromoacetyl chlorideHCID 89602—
반응물(3,4-Dimethyl-phenyl)-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-amineHCID 58007591—
용매Diethyl EtherHCID 3283—
용매tert-Butyl methyl etherHCID 15413—
생성물2-Bromo-N-(3,4-dimethyl-phenyl)-N-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-acetamideHCID 5800760243%

반응 단계

A solution of (3,4-dimethyl-phenyl)-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-amine (220 mg, 0.75 mmol) in diethylether (2 mL) was cooled to 0° C. and triethylamine (114 μL, 0.82 mmol) and bromoacetyl chloride (81 μL, 0.97 mmol) were added. After stirring for 15 min. at this temperature the ice bath was removed and the suspension was stirred for 2 h at ambient temperature. Further bromoacetyl chloride (16 μL, 0.2 mmol) was added and the resulting suspension was stirred for 1 h at this temperature. It was diluted with TBME (10 mL) and washed with water (15 mL) and brine (15 mL). The combined aqueous layers were extracted with TBME (15 mL) and the combined organic layers dried over sodium sulfate. Concentration and purification by chromatography (SiO2, heptane:ethyl acetate=95:5 to 70:30) afforded the title compound (134 mg, 43%) as a light brown oil. MS m/e: 417.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08133909B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-1689b8c1754f4310bc5d7f48edbf9a13
출처 메모uspto-grants-2012_03