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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 716642생성일: 2026년 10월 25일

Trifluoroacetic acid → Alanine--lysine (1/1)

https://huagongshe.com/reaction/716642

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물ThioanisoleHCID 7520—
반응물N-carboxy-N'-benzyloxycarbonyl-L-lysine anhydrideHCID 86718959—
반응물(2S)-2-amino-6-(phenylmethoxycarbonylamino)hexanoic acid;(2S)-2-aminopropanoic acidHCID 131734145—
생성물Alanine--lysine (1/1)HCID 168589—

반응 단계

To the poly-L-alanine/Nε-benzyloxycarbonyl-L-lysine copolymer (9/1) obtained in Production Example 16 were added 270 equivalents and 5 equivalents of trifluoroacetic acid (manufactured by TOKYO CHEMICAL INDUSTRY CO., LTD.) and thioanisole (manufactured by TOKYO CHEMICAL INDUSTRY CO., LTD.), respectively, relative to the number of moles of N-carboxy-N′-benzyloxycarbonyl-L-lysine anhydride, and the mixture was reacted at room temperature to give a poly-L-alanine/L-lysine copolymer. This was dissolved in a dichloromethane-trifluoroacetic acid mixed solvent (50:70 (v/v)) to give a 4.4 wt % poly-L-alanine/L-lysine copolymer solution. A fiber structure made of a poly-L-alanine/L-lysine copolymer was obtained from this solution in the same manner as in Production Example 1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09192624B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-b83c5b18197a49fb9342300b9b74c3ec
출처 메모uspto-grants-2015_11