Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25280생성일: 2026년 10월 23일
Potassium Carbonate → (2-Ethoxymethoxy-5-(4-trifluoromethylphenyl)phenyl] 2,2,2-trifluoroethyl sulfide
https://huagongshe.com/ko/reaction/25280
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1,1,1-Trifluoro-2-iodoethane | HCID 67709 | — |
| 반응물 | 1,1'-Thiodi-[2-ethoxymethoxy-5-(4-trifluoromethylphenyl)benzene] | HCID 22170890 | — |
| 반응물 | Sodium Formaldehyde Sulfoxylate | HCID 23689980 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (2-Ethoxymethoxy-5-(4-trifluoromethylphenyl)phenyl] 2,2,2-trifluoroethyl sulfide | HCID 86587598 | 151.1% |
반응 단계
3.3 g (5.0 mmol) of 1,1′-thiodi-[2-ethoxymethoxy-5-(4-trifluoromethylphenyl)benzene], 3.0 g (19.5 mmol) of Rongalite, 3.0 g (21.7 mmol) of potassium carbonate and 3.2 g (17.6 mmol) of 2,2,2-trifluoroethyl iodide were stirred in 50 ml of N,N-dimethylformamide at room temperature for 3 hours. The resulting reaction mixture was poured into 300 ml of water and extracted with 50 ml of ethyl acetate twice. The ethyl acetate layer was washed with 50 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 3.1 g of (2-ethoxymethoxy-5-(4-trifluoromethylphenyl)phenyl] 2,2,2-trifluoroethyl sulfide (yield 75.6%) as a pale yellow viscous liquid (nD20 1.5213).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06858639B2 |
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| 출처 데이터셋 | uspto-grants-2005_02 |
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| ORD ID | ord-c3157614ddee40f7b889ddcb92241301 |
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| 출처 메모 | uspto-grants-2005_02 |
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