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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 429268생성일: 2026년 10월 26일

Formaldehyde → 5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(2,5-dihydro-2-methyl-1,2,4-oxadiazol-3-yl)-4-trifluoromethylsulfinylpyrazole

https://huagongshe.com/reaction/429268

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(N-hydroxy-N-methylamidino)-4-trifluoromethylsulfinylpyrazoleHCID 11070934—
촉매Acetic AcidHCID 176—
용매AcetonitrileHCID 6342—
생성물5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(2,5-dihydro-2-methyl-1,2,4-oxadiazol-3-yl)-4-trifluoromethylsulfinylpyrazoleHCID 1835478325.1%

반응 조건

온도50 °C

반응 단계

5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(N-hydroxy-N-methylamidino)-4-trifluoromethylsulfinylpyrazole(1.00 g, 2.07 mmol) was dissolved in 10 ml of acetonitrile, and then aqueous 37% formaldehyde solution 840 mg (10.3 mmol) and 5 drops of acetic acid were added. After the mixture was stirred at 50° C. for 5 hours, aqueous 37% formaldehyde solution 840 mg (10.3 mmol) and, 5 drops of acetic acid were further added, followed by stirring at 50° C. for 5 hours. The reaction mixture was concentrated in vacuo and to the residual oil was added ethyl acetate, and then washed twice with an aqueous saturated sodium hydrogencarbonate solution, once with an aqueous saturated sodium chloride solution. After drying over anhydrous magnesium sulfate, the solvent was distilled off. The resulting concentrated residue was purified by silica gel column chromatography [eluent: mixed solvent of ethyl acetate and n-hexane (volume ratio=1:2)] to obtain 260 mg (0.52 mmol) of the title compound as a colorless crystal. Yield 25%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06316477B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-ea7655438afb498ead8192fda7830f09
출처 메모uspto-grants-2001_11