Реакция #50733

Уравнение реакции

H-Asn-OH.H2O

THF

triethylamine

Boc-Ser(Bzl)-OSu

→

Boc-Ser(Bzl)-Asn-OH

Выход 71.2%

Растворители

H2O

Условия реакции

Обработка

1. 1
   Температураcooling
2. 2
   workup.DISTILLATIONafter which the THF was distilled off
3. 3
   Температураcooling
4. 4
   Экстракцияthe resulting oily product was extracted with 200 ml of ethyl acetate
5. 5
   ПромывкаThe extract was washed with 50 ml of saturated aqueous sodium chloride solution twice
6. 6
   Сушкаdried over anhydrous sodium sulfate
7. 7
   Концентрированиеconcentrated under reduced pressure
8. 8
   workup.ADDITIONThe residue was treated with ether/petroleum ether (2:1) for solidification
9. 9
   Другоеthe resultant powder was reprecipitated from methanol-isopropyl ether

Методика

In 80 ml of H2O was suspended 4.50 g of H-Asn-OH.H2O, followed by addition of 80 ml of a THF solution containing 4.20 ml of triethylamine and 14.13 g of Boc-Ser(Bzl)-OSu under ice-cooling. The mixture was stirred at room temperature for 20 hours, after which the THF was distilled off. The residual aqueous solution was adjusted to pH 3 with 1M citric acid under ice-cooling and the resulting oily product was extracted with 200 ml of ethyl acetate. The extract was washed with 50 ml of saturated aqueous sodium chloride solution twice, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was treated with ether/petroleum ether (2:1) for solidification and the resultant powder was reprecipitated from methanol-isopropyl ether to give 8.74 g of Boc-Ser(Bzl)-Asn-OH (yield 71.2%).

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