HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Hexenoic Acid → (3r,3Ar,6r,6ar)-6-hydroxyhexahydrofuro[3,2-b]furan-3-yl hex-5-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Hexenoic Acid | HCID 15308 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1,4:3,6-Dianhydro-D-mannitol | HCID 10975624 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3r,3Ar,6r,6ar)-6-hydroxyhexahydrofuro[3,2-b]furan-3-yl hex-5-enoate | HCID 59509518 | — |
Reaction Steps
To a stirred solution of 1,4:3,6-dianhydro-D-mannitol (isommanide) (2.00 g, 13.68 mmol), 5-hexenoic acid (1.60 g, 13.68 mmol) and DMAP (0.17 g, 1.4 mmol) in DCM (50 mL) cooled at 0° C., EDAC (3.1 g, 16.42 mmol) was added. The solution was stirred at room temperature for 6 hrs. The solution was diluted with DCM (30 mL), washed with a solution of NaHPO4 5% (2×40 mL) and brine. The organic layer was dried over sodium sulfate and concentrated under vacuo. The residue was purified by flash chromatography (Biotage SP1, 40+M column, TLC method: n-Hexane/EtOAc −8:2, Rf product: 0.35) yielding the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08003811B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-8dfa0bc0a97a408db47c58e270018a49 |
| Source note | uspto-grants-2011_08 |