HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → (3,4,5,6-Tetrahydroxytetrahydropyran-2-ylmethyl)10,12-tricosadiynoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 10,12-Tricosadiynoic Acid | HCID 538457 | — |
| Reactant | 1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranose | HCID 2723629 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3,4,5,6-Tetrahydroxytetrahydropyran-2-ylmethyl)10,12-tricosadiynoate | HCID 53883249 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05567413 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-99c35bd0113f409aadcc4e2cb047536f |
| Source note | uspto-grants-1996_10 |