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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 865620생성일: 2026년 10월 24일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → (3,4,5,6-Tetrahydroxytetrahydropyran-2-ylmethyl)10,12-tricosadiynoate

https://huagongshe.com/ko/reaction/865620

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물10,12-Tricosadiynoic AcidHCID 538457—
반응물1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranoseHCID 2723629—
용매DichloromethaneHCID 6344—
생성물(3,4,5,6-Tetrahydroxytetrahydropyran-2-ylmethyl)10,12-tricosadiynoateHCID 53883249—

반응 단계

1,2;3,4-di-O-isopropylidene-D-galactopyranose (2.6 g, 10 mmol) and 10,12-tricosadiynoic acid (3.5 g, 10 mmol) were dissolved in 25 ml methylene chloride. 1-Ethyl-3(3-dimethylaminopropyl)carbodiimide (2 g, >10 mmol) was added neat. The reaction mixture was stirred overnight at room temperature. The reaction mixture was diluted to 100 ml, extracted with water (2×25 ml), dried over MgSO4 and the solvent was removed in vacuo. The crude product was treated with trifluoroacetic acid (10 ml) at room temperature for 30 minutes, evaporated in vacuo, and purified by straight phase chromatography on a CHROMATOTRON, eluted with methanol/chloroform (5:95). The product was characterised by NMR.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05567413
출처 데이터셋uspto-grants-1996_10
ORD IDord-99c35bd0113f409aadcc4e2cb047536f
출처 메모uspto-grants-1996_10