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HRID 1734976作成日:2026年10月27日

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

https://huagongshe.com/reaction/1734976

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物10,12-Tricosadiynoic AcidHCID 538457—
反応物1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranoseHCID 2723629—
溶媒DichloromethaneHCID 6344—
生成物(3,4,5,6-Tetrahydroxytetrahydropyran-2-ylmethyl)10,12-tricosadiynoateHCID 53883249—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05536490
出典データセットuspto-grants-1996_07
ORD IDord-2ac825b716854fec844741f4928ead05
出典メモuspto-grants-1996_07