Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 743744생성일: 2026년 10월 23일
Methanol → 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-Heptadecafluorooctane
https://huagongshe.com/ko/reaction/743744
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Perfluorooctyl iodide | HCID 10491 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 촉매 | Tetrabutylphosphonium bromide | HCID 76564 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-Heptadecafluorooctane | HCID 101652 | 93.8% |
반응 단계
Into a 1 l four-necked flask equipped with a stirrer, a reflux condenser, a dropping funnel and a thermometer, 250 cc of methanol and 3 g of tetrabutylphosphonium bromide and 74.3 g (1.1 mols) of 85% potassium hydroxide were charged. The reactor was heated to bring the internal temperature to 60° C. Then, 273 g (0.5 mol) of C8F17I was dropwise added thereto over a period of one hour. After completion of the dropwise addition, heating and refluxing were continued for 8 hours. The conversion at that time was 99.6%. The reactor was cooled to room temperature. Then, 300 g of water was added to dissolve precipitated potassium iodide. The crude reaction solution was separated into two layers, and the fluorocarbon layer (lower layer) was further washed with 300 g of water to recover a fluorocarbon. Thus, 197 g of C8F17H having a purity of 99.0%, was obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05557017 |
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| 출처 데이터셋 | uspto-grants-1996_09 |
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| ORD ID | ord-f45f070299654fe2afd5ae6ec1f9ba6d |
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| 출처 메모 | uspto-grants-1996_09 |
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