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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | 5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(N-hydroxy-N-methylamidino)-4-trifluoromethylsulfinylpyrazole | HCID 11070934 | — |
| 촉매 | Acetic Acid | HCID 176 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(2,5-dihydro-2-methyl-1,2,4-oxadiazol-3-yl)-4-trifluoromethylsulfinylpyrazole | HCID 18354783 | 25.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06316477B1 |
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| 출처 데이터셋 | uspto-grants-2001_11 |
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| ORD ID | ord-ea7655438afb498ead8192fda7830f09 |
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| 출처 메모 | uspto-grants-2001_11 |
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