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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1096027생성일: 2026년 10월 27일

Hydrochloric Acid → 4-{3-Chloro-4-[2-(1,5-dimethyl-6-oxo-1,6-dihydro-pyridin-3-yl)-3,3,3-trifluoro-2-hydroxy-1-methyl-propyl]-phenoxy}-2-trifluoromethyl-benzoic acid

https://huagongshe.com/reaction/1096027

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium ChloriteHCID 23668197—
반응물4-{3-Chloro-4-[2-(1,5-dimethyl-6-oxo-1,6-dihydro-pyridin-3-yl)-3,3,3-trifluoro-2-hydroxy-1-methyl-propyl]-phenoxy}-2-trifluoromethyl-benzaldehydeHCID 86645956—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
용매2-Methyl-2-buteneHCID 10553—
생성물4-{3-Chloro-4-[2-(1,5-dimethyl-6-oxo-1,6-dihydro-pyridin-3-yl)-3,3,3-trifluoro-2-hydroxy-1-methyl-propyl]-phenoxy}-2-trifluoromethyl-benzoic acidHCID 7231055596.2%

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온도0 °C

반응 단계

To a solution of 4-{3-chloro-4-[2-(1,5-dimethyl-6-oxo-1,6-dihydro-pyridin-3-yl)-3,3,3-trifluoro-2-hydroxy-1-methyl-propyl]-phenoxy}-2-trifluoromethyl-benzaldehyde (105 mg) in tert.-butanol (1 ml) and 2-methyl-2-butene (0.12 ml) was added a solution of sodium chlorite (28 mg) and sodiumdihydrogenphosphate-dihydrate (34 mg) in water (0.8 ml) at 0° C. The mixture was stirred for 10 minutes at 0° C. and for 4.5 h at room temperature. The mixture was acidified with 1 M aqueous HCl and extracted with ethyl acetate. The organic phase was dried (MgSO4), filtered and concentrated to give the title compound (104 mg) as a colorless solid. MS (m/e, ISP neg. ion)=562.1 [M−H+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08138189B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-724238be05dc42d7a71b0dfdee80fbe8
출처 메모uspto-grants-2012_03