Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 364778생성일: 2026년 10월 26일
Potassium Iodide → 1-(3-Trifluoromethylphenyl)-1-[4-(diethylcarbamoylmethoxy)-phenyl]-propan-1-ol
https://huagongshe.com/reaction/364778
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Chloro-N,N-diethylacetamide | HCID 16844 | — |
| 반응물 | 3-Trifluoromethyl-4'-hydroxy-alpha-ethylbenzhydrol | HCID 181876 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 1-(3-Trifluoromethylphenyl)-1-[4-(diethylcarbamoylmethoxy)-phenyl]-propan-1-ol | HCID 20207217 | — |
반응 단계
14.8 g. 1-(3-trifluoromethylphenyl)-1-(4-hydroxyphenyl)-propan-1-ol, 7.6 g. of anhydrous potassium carbonate, 2 g. of potassium iodide, 8.2 g. of monochloroacetic acid diethylamide and 150 ml. of dry acetone are boiled for 5 hours, under stirring. The reaction mixture is cooled and the solvent is distilled off under reduced pressure. To the residue water is added and it is extracted with benzene. The benzene phase is shaken with water and subsequently a 5% aqueous sodium hydroxide solution and washed to neutral with water. It is dried over anhydrous sodium sulfate, filtered off and the solution is evaporated in vacuo. The solid residue is crystallized from a mixture of n-hexane and ethyl acetate. 17.6 g. of the named compound are obtained, melting at 83°-84° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04605785 |
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| 출처 데이터셋 | uspto-grants-1986_08 |
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| ORD ID | ord-7d338cd0b7ea4d9b862df2ab907ad556 |
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| 출처 메모 | uspto-grants-1986_08 |
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