Реакция #710554

Уравнение реакции

tert-butyl 2-((tert-butyldimethylsilyloxy)methyl)-3-fluoroallylcarbamate

TBAF

→

(E)-tert-butyl 3-fluoro-2-(hydroxymethyl)allylcarbamate

Выход 15.6%

(Z)-tert-butyl 3-fluoro-2-(hydroxymethyl)-allylcarbamate

Выход 6.5%

Растворители

THF

Условия реакции

Обработка

1. 1
   workup.WAITThe resulting solution was left
2. 2
   ДругоеThe reaction mixture was partitioned between water (70 mL) and ethyl acetate (50 mL)
3. 3
   ЭкстракцияThe aqueous layer was extracted with ethyl acetate (50 mL)
4. 4
   Промывкаthe combined organics were washed with saturated aqueous NH4Cl (70 mL)
5. 5
   СушкаAfter drying over Na2SO4
6. 6
   Концентрированиеthe organics were concentrated in vacuo
7. 7
   ДругоеPurification of the crude material over silica gel eluting with 20% ethyl acetate and 5% THF in n-hexane

Методика

To a stirring solution of tert-butyl 2-((tert-butyldimethylsilyloxy)methyl)-3-fluoroallylcarbamate (E/Z=1:1; 12.0 g, 37.6 mmol) in THF (30 mL) at room temperature was added TBAF (1:0 M in THF; 45.1 mL, 45.1 mmol). The resulting solution was left to stir for 30 min. The reaction mixture was partitioned between water (70 mL) and ethyl acetate (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL) and the combined organics were washed with saturated aqueous NH4Cl (70 mL) followed by brine (70 mL). After drying over Na2SO4, the organics were concentrated in vacuo. Purification of the crude material over silica gel eluting with 20% ethyl acetate and 5% THF in n-hexane gave (Z)-tert-butyl 3-fluoro-2-(hydroxymethyl)-allylcarbamate (0.5 g, 6.5%), (E)-tert-butyl 3-fluoro-2-(hydroxymethyl)allylcarbamate (1.2 g, 15.6%) and a mixture of the E/Z isomers (5.5 g, 71.4%).

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