HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055501Generated: October 31, 2026
2-Iodoxybenzoic acid → HCID 117928482, compound
https://huagongshe.com/reaction/1055501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Iodoxybenzoic acid | HCID 108794 | — |
| Reactant | HCID 67153941 | HCID 67153941 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 117928482 | HCID 117928482 | 60% |
Reaction Steps
To a solution of [(1S,2S,3S,4R,5S)-2,3,4-tribenzyloxy-5-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-6,8-dioxabicyclo[3.2.1]octan-1-yl]methanol 1j (8.53 g, 12.08 mmol) in dichloromethane (350 mL) was added 2-iodoxybenzoicacid (6.77 g, 24.2 mmol) at room temperature. The mixture was refluxed at 45° C. for 36 hours and quenched with 150 mL of water. The mixture was partitioned between dichloromethane and water. The organic layer was washed with saturated aqueous sodium chloride (150 mL×2), dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by silica gel chromatography eluted with PE/EtOAc(v/v)=10/1 to give the title compound 1k as pale yellow oil (4.94 g, 60.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394329B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-4aca6ec68f3e4933a5175ceacdc1d745 |
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| Source note | uspto-grants-2016_07 |
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