반응 #50733

반응 방정식

H-Asn-OH.H2O

THF

triethylamine

Boc-Ser(Bzl)-OSu

→

Boc-Ser(Bzl)-Asn-OH

수율 71.2%

용매

H2O

반응 조건

후처리

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

실험 절차

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%).

출처