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HRID 49365생성일: 2026년 10월 23일

Hexafluoroacetone → (e)-6-{5-[3,4-Bis(tert-butyldimethylsilanyloxy-methyl)phenoxymethyl]-2-thienyl}-1,1,1-trifluoro-2-trifluoromethyloct-5-en-3-yn-2-ol

https://huagongshe.com/ko/reaction/49365

반응식

참여 물질

역할이름HCID투입량
반응물HexafluoroacetoneHCID 12695—
반응물2-[3,4-bis(tert-butyldimethylsilanyloxymethyl)phenoxymethyl]-5-((E)-1-ethyl-but-1-en-3-ynyl)thiopheneHCID 88012139—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(e)-6-{5-[3,4-Bis(tert-butyldimethylsilanyloxy-methyl)phenoxymethyl]-2-thienyl}-1,1,1-trifluoro-2-trifluoromethyloct-5-en-3-yn-2-olHCID 20636349—

반응 조건

온도-78 °C

반응 단계

1.7 g (3 mmol) of 2-[3,4-bis(tert-butyldimethylsilanyloxymethyl)phenoxymethyl]-5-((E)-1-ethyl-but-1-en-3-ynyl)thiophene are dissolved in 50 mL of THF and the mixture is cooled to −78° C. 1.3 mL (3.3 mmol) of 2.5 M butyllithium are then added. After stirring for 15 minutes at the same temperature, a gentle flow of hexafluoroacetone (gas) is introduced into the reaction medium. After reaction for 20 minutes at −78° C., the flow of gas is stopped and the reaction medium is treated in the usual manner. The residue obtained is purified by chromatography on silica gel. The desired product is obtained in the form of a yellow oil (1 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706725B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-22abab40fc7b49eeb1a7d05376d358b9
출처 메모uspto-grants-2004_03