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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 345617생성일: 2026년 10월 25일

Phenol → 2-(2-Phenoxytetrafluoro-ethyl)-1,3-dioxolane

https://huagongshe.com/reaction/345617

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물TetrafluoroethyleneHCID 8301—
반응물Sodium hydrideHCID 24758—
반응물2-Chloroethyl formateHCID 246748—
용매WaterHCID 962—
용매DiglymeHCID 8150—
생성물2-(2-Phenoxytetrafluoro-ethyl)-1,3-dioxolaneHCID 1440145057%

반응 단계

A suspension of 17.3 g (0.36 mol) of 50% NaH in mineral oil in 100 mL of diglyme was treated with a solution of 33.9 g (0.36 mol) of phenol in 50 mL of diglyme. The resulting mixture was stirred overnight and then charged into a 400 mL metal tube along with 38.6 g (0.36 mol) of 2-chloroethyl formate and 40 g (0.40 mol) of tetrafluoroethylene. The resulting mixture was agitated for 12 h, and then added to 1 L of cold water, thereby causing the formation of layers. The lower layer was washed with water, dried over CaSO4, and distilled to afford 54.5 g (57% yield) of 2-(2-phenoxytetrafluoro-ethyl)-1,3-dioxolane, b.p. 62°-65° at 8 Pa (0.06 mm). The IR (neat) and NMR (CCl4) spectra of the product were consistent with the assigned structure. Anal.: Calcd. for C11H10F4O3 :C, 49.63; H, 3.79l F, 28.55. Found: C, 49 90; H, 3.80; F, 28.91.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05057586
출처 데이터셋uspto-grants-1991_10
ORD IDord-1ef80adf2f2241d58d016862f4c661db
출처 메모uspto-grants-1991_10