Реакция #1340604

Уравнение реакции

hydrochloric acid

diethyl ether

(3S,4S)-1-benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-formylpyrrolidine

diiodomethane

→

title compound

(3S,4S)-1-Benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-vinylpyrrolidine

Растворители

tetrahydrofuran

tetrahydrofuran

tetrahydrofuran

Условия реакции

Обработка

1. 1
   workup.WAITover 8 minutes
2. 2
   Другоеthereof was elevated to room temperature
3. 3
   workup.WAITover 7 minutes
4. 4
   workup.STIRRINGby stirring for 1.5 hours
5. 5
   ТемператураSubsequently, under cooling with ice
6. 6
   ЭкстракцияThe obtained aqueous layer was extracted with diethyl ether (100 mL×2)
7. 7
   ПромывкаThe combined organic layer was washed by saturated brine (100 mL)
8. 8
   Сушкаdried over anhydrous sodium sulfate
9. 9
   Фильтрацияfiltered
10. 10
    Концентрированиеconcentrated under reduced pressure
11. 11
    ДругоеThe obtained residue was purified through silica gel column chromatography (ethyl acetate:n-hexane=1:3)

Методика

Under cooling with ice, titanium tetrachloride (3.30 mL, 1.0M toluene solution) was added to a suspension of zinc powder (1.86 g, 28.5 mmol) in tetrahydrofuran (15 mL) over 2 minutes, followed by stirring for 5 minutes at the same temperature. A solution of diiodomethane (1.15 mL, 14.3 mL) in tetrahydrofuran (5 mL) was added thereto over 8 minutes, and the resultant mixture was stirred for 15 minutes while the temperature thereof was elevated to room temperature. A solution of (3S,4S)-1-benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-formylpyrrolidine (900 mg, 2.58 mmol) in tetrahydrofuran (5.0 mL) was added thereto over 7 minutes, followed by stirring for 1.5 hours. Subsequently, under cooling with ice, the resultant mixture was poured to 0.5 mol/L hydrochloric acid (10 mL), followed by dilution with diethyl ether (60 mL). The obtained aqueous layer was extracted with diethyl ether (100 mL×2). The combined organic layer was washed by saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure. The obtained residue was purified through silica gel column chromatography (ethyl acetate:n-hexane=1:3), to thereby yield the title compound as a colorless oily substance (3.09 g, 31%).

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