Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1284927생성일: 2026년 10월 27일
Butyl isocyanate → 1-(3-Trifluoromethylphenyl)-1-(4-butylaminocarbonyloxyphenyl)-1-propanol
https://huagongshe.com/reaction/1284927
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butyl isocyanate | HCID 8110 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 3-Trifluoromethyl-4'-hydroxy-alpha-ethylbenzhydrol | HCID 181876 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 1-(3-Trifluoromethylphenyl)-1-(4-butylaminocarbonyloxyphenyl)-1-propanol | HCID 14727324 | — |
반응 단계
8.9 g. of 3-trifluoromethyl-4'-hydroxy-α-ethyl-benzhydrol, 3.3 g. of n-butyl-isocyanate and 0.06 ml. of triethyl amine in 45 ml. of dry benzene are heated up to 50° C. under stirring, and the reaction mixture is kept at the same temperature for one additional hour. The progress of the reaction is monitored by thin layer chromatography. When the reaction is complete, the mixture is cooled to room temperature, the benzene solution is shaken with a 5% aqueous potassium hydroxide solution and washed to neutral with water. The organic phase is dried over anhydrous magnesium sulfate, filtered, and the solvent is distilled off under reduced pressure. The solid residue is crystallized from a mixture of ethyl acetate and n-hexane. 11.4 g. of the named compound are obtained, melting at 99° to 100° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04564630 |
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| 출처 데이터셋 | uspto-grants-1986_01 |
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| ORD ID | ord-f076cec6be3d4570b8a05b9fb53c40d8 |
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| 출처 메모 | uspto-grants-1986_01 |
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