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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22455생성일: 2026년 10월 25일

Tetrahydrofuran → Boc-Ser(Bzl)-Asn-OH

https://huagongshe.com/reaction/22455

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물TriethylamineHCID 8471—
반응물L-Asparagine, monohydrateHCID 170358—
반응물Boc-Ser(Bzl)-OSuHCID 12879025—
용매WaterHCID 962—
생성물Boc-Ser(Bzl)-Asn-OHHCID 1528319971.2%

반응 단계

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 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428129
출처 데이터셋uspto-grants-1995_06
ORD IDord-5fa9ef88a1ae49ccabd1b265975312d0
출처 메모uspto-grants-1995_06