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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965923Generated: November 2, 2026

Water → 3-tert-butyl-5-iodosalicylaldehyde

https://huagongshe.com/reaction/1965923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-tert-Butyl-2-hydroxybenzaldehydeHCID 3678675—
ReactantTrimethylbenzylammonium DichloroiodateHCID 56924451—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product3-tert-butyl-5-iodosalicylaldehydeHCID 12034504—

Reaction Steps

3-tert-butyl salicylaldehyde (1) (8.4 mmol) was dissolved in 100 ml of a mixture of methanol and methylene chloride (3:7). Benzyltrimethylammonium dichloroiodate (3.23 g; 9.2 mmol) and water free calcium carbonate (1.1 g; 11 mmol) were added. After two hours, the excess of calcium carbonate was filtered off. After removal of about 80% of the solvent, 20 ml of a sodium hydrogensulfite solution (5%) was added decolourizing the mixture. Extraction with diethyl ether, drying over sodium sulphate and removal of the solvent yielded the aldehyde as raw product. Purification by recrystallization from n-pentane produced 3-tert-butyl-5-iodosalicylaldehyde in a 48% yield as yellow crystals which are slightly light sensitive and should be stored in the dark.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420563B2
Source datasetuspto-grants-2013_04
ORD IDord-1a2034d00123467f8753b696c71e2e3f
Source noteuspto-grants-2013_04