HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Iodoxybenzoic acid → (1S,2S,3S,4R,5S)-2,3,4-tribenzyloxy-5-[4-chloro-3-[(2,3-difluoro-4-methoxy-phenyl)methyl]phenyl]-6,8-dioxabicyclo[3.2.1]octane-1-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Iodoxybenzoic acid | HCID 108794 | — |
| Reactant | [(1S,2S,3S,4R,5S)-2,3,4-tribenzyloxy-5-[4-chloro-3-[(2,3-difluoro-4-methoxy-phenyl)methyl]phenyl]-6,8-dioxabicyclo[3.2.1]octan-1-yl]methanol | HCID 86685114 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (1S,2S,3S,4R,5S)-2,3,4-tribenzyloxy-5-[4-chloro-3-[(2,3-difluoro-4-methoxy-phenyl)methyl]phenyl]-6,8-dioxabicyclo[3.2.1]octane-1-carbaldehyde | HCID 122610446 | 105.2% |
Reaction Steps
To a solution of [(1S,2S,3S,4R,5S)-2,3,4-tribenzyloxy-5-[4-chloro-3-[(2,3-difluoro-4-methoxy-phenyl)methyl]phenyl]-6,8-dioxa bicyclo[3.2.1]octan-1-yl]methanol 210 (0.52 g, 0.68 mmol) in ethyl acetate (20 mL) was added 2-iodoxybenzoic acid (0.58 g, 2.06 mmol) at room temperature. The mixture was refluxed for 20 hours and cooled to room temperature, then filtered. The filtrate was concentrated in vacuo to give the title compound 21p as a white solid (0.52 g, 100%). This material was not further purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09394329B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-b48239fc239c4b93b2d5fd3181528b47 |
| Source note | uspto-grants-2016_07 |