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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403011Generated: October 26, 2026

Iodine → 3,4-Dibenzyloxy-6-iodobenzyl alcohol

https://huagongshe.com/reaction/403011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant3,4-Bis(benzyloxy)benzyl alcoholHCID 74338—
CatalystSilver trifluoroacetateHCID 76299—
SolventChloroformHCID 6212—
Product3,4-Dibenzyloxy-6-iodobenzyl alcoholHCID 6673355084%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742139B2
Source datasetuspto-grants-2014_06
ORD IDord-ecb27ec953764accb3730e698a8568d6
Source noteuspto-grants-2014_06