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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 623960생성일: 2026년 10월 24일

Water → 1-(2-Amino-5-bromophenyl)-2,2,2-trifluoroethanone

https://huagongshe.com/ko/reaction/623960

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium SulfateHCID 24436—
반응물Stannous ChlorideHCID 24479—
반응물Sodium AzideHCID 33557—
반응물1-(5-Bromo-2-fluorophenyl)-2,2,2-trifluoroethan-1-oneHCID 11369266—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
생성물1-(2-Amino-5-bromophenyl)-2,2,2-trifluoroethanoneHCID 46838802—

반응 단계

A solution of 1-(5-bromo-2-fluorophenyl)-2,2,2-trifluoroethanone (6.67 g, 24.6 mmol, Intermediate 7, step a) in DMSO (6.2 mL) was treated with NaN3 (1.76 g, 27.0 mmol) and stirred under air (lightly capped) at 95° C. for 1 hour. The brownish-red opaque reaction was then cooled to room temperature on an ice bath, diluted with EtOAc (49 mL), treated with SnCl2.dihydrate (6.66 g, 29.5 mmol) in several portions over ˜30 seconds followed by water (1.33 mL, 73.8 mmol), and the mixture was stirred at room temperature for 30 minutes. The reddish solution with heavy off-white particulates was then treated with anhydrous Na2SO4 (˜6 g) and stirred vigorously for a few minutes. The mixture was then filtered over a bed of Celite®, and the cloudy orange filtrate was dry load flash chromatographed (˜60 g silica gel) with a heptane to 50% DCM/heptane gradient to provide the title compound as an orange oil that crystallized upon standing.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09303015B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-1d8c596e31ed4188837c97f9a443a05d
출처 메모uspto-grants-2016_04