HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Iodoxybenzoic acid → (1S,2S,3S,4R,5S)-2,3,4-tribenzyloxy-5-[4-chloro-3-[[4-(trifluoromethoxy) 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-[[4-(trifluoromethoxy)phenyl]methyl]phenyl]-6,8-dioxabicyclo[3.2.1]octan-1-yl]methanol | HCID 86685144 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (1S,2S,3S,4R,5S)-2,3,4-tribenzyloxy-5-[4-chloro-3-[[4-(trifluoromethoxy) phenyl]methyl]phenyl]-6,8-dioxabicyclo[3.2.1]octane-1-carbaldehyde | HCID 118377816 | 101.4% |
Reaction Steps
To a solution of [(1S,2S,3S,4R,5S)-2,3,4-tribenzyloxy-5-[4-chloro-3-[[4-(trifluoromethoxy)phenyl]methyl]phenyl]-6,8-dioxabicyclo[3.2.1]octan-1-yl]methanol 15o (0.7 g, 0.94 mmol) in ethyl acetate (30 mL) was added 2-iodoxybenzoic acid (0.79 g, 2.81 mmol) at room temperature. The mixture was refluxed for 24 hours and filtered. The filtrate was washed with saturated aqueous sodium bicarbonate (10 mL×2) and saturated aqueous sodium chloride (10 mL×2) in turn, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to give the title compound 15p as yellow oil (0.71 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-bd92a527b62047e9a06381f3fa5762df |
| Source note | uspto-grants-2016_07 |