Реакция #77643

Уравнение реакции

hexafluoroacetone

2-[3,4-bis(tert-butyldimethylsilanyloxymethyl)phenoxymethyl]-5-((E)-1-ethyl-but-1-en-3-ynyl)thiophene

butyllithium

→

desired product

(E)-6-{5-[3,4-bis(tert-Butyldimethylsilanyloxy-methyl)phenoxymethyl]-2-thienyl}-1,1,1-trifluoro-2-trifluoromethyloct-5-en-3-yn-2-ol

Растворители

THF

Условия реакции

Обработка

1. 1
   ДругоеAfter reaction for 20 minutes at −78° C.
2. 2
   workup.ADDITIONthe reaction medium is treated in the usual manner
3. 3
   ДругоеThe residue obtained
4. 4
   Другоеis purified by chromatography on silica gel

Методика

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).

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