HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 3,4-Dibenzyloxy-6-iodobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 3,4-Bis(benzyloxy)benzyl alcohol | HCID 74338 | — |
| Catalyst | Silver trifluoroacetate | HCID 76299 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3,4-Dibenzyloxy-6-iodobenzyl alcohol | HCID 66733550 | 84% |
Reaction Steps
The dibenzyloxybenzyl alcohol 28 (21.44 mmol) and silver trifluoroacetate (21.44 mmol) were suspended in 100 mL of dry chloroform and stirred under argon. A solution of iodine (21.44 mmol) in dry chloroform (50 mL) was added to the suspension dropwise at room temperature. The reaction mixture was then stirred for a further period of 2 h and filtered. The filtrate was washed with 20% sodium thiosulfate solution in water. The organic layer was separated and dried over anhydrous Na2SO4. Filtration was followed by evaporation of the chloroform solution resulting in the pure iodo compound, 3,4-Dibenzyloxy-6-iodobenzyl alcohol (29), as a pale yellow solid in 84% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08742139B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-ecb27ec953764accb3730e698a8568d6 |
| Source note | uspto-grants-2014_06 |