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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12401생성일: 2026년 10월 24일

Triethylamine → (R)-(+)-3-Benzyloxy-2-(Boc-amino)-1-propanol

https://huagongshe.com/ko/reaction/12401

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)-HCID 90234—
용매TetrahydrofuranHCID 8028—
생성물(R)-(+)-3-Benzyloxy-2-(Boc-amino)-1-propanolHCID 1106587389.2%

반응 단계

O-benzyl-N-(t-butoxycarbonyl)-L-serine (2 g) was dissolved in tetrahydrofuran (20 ml), triethylamine (1.22 ml) was added, and ethyl chloroformate (713 μl) was further added dropwise at 0° C. After stirring the reaction mixture at room temperature for 30 min, the reaction mixture was filtered, and one piece of ice was added to the filtrate. Sodium borohydride (515 mg) was further added, and the mixture was stirred at room temperature for 6 hrs. The reaction mixture was diluted with ethyl acetate and, after washing with water, the organic layer was dried over anhydrous sodium sulfate. The solvent was evaporated and the obtained crude product was purified by silica gel chromatography (ethyl acetate-hexane) to give t-butyl (1R)-2-(benzyloxy)-1-(hydroxymethyl)ethylcarbamate (1.7 g)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728005B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-62c17d1cfb3e4e06b586c994edd4847a
출처 메모uspto-grants-2010_06