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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965924Generated: November 3, 2026

p-Toluenesulfonic acid → HCID 136388724, compound

https://huagongshe.com/reaction/1965924

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-IodoanilineHCID 10893—
ReactantSodium BicarbonateHCID 516892—
Reactant3-tert-Butyl-2-hydroxybenzaldehydeHCID 3678675—
SolventTolueneHCID 1140—
ProductHCID 136388724HCID 13638872496%

Reaction Steps

An amount of 5.84 mmol of 3-tert-butyl salicylaldehyde (1) (1.04 g/1 ml) was dissolved in 150 ml of toluene. After addition of 4-iodoaniline (1.53 g/7 mmol/1.2 equivs.) and a few crystals of para-toluenesulfonic acid, the reaction mixture was stirred under reflux for three hours applying a Dean-Stark-trap. After cooling down to room temperature, sodium hydrogencarbonate solution (150 ml) was added. The organic phase was separated and filtered over sodium sulphate and silica. Removing the solvent and recrystallization from ethanol at −20° C. gave the title compound in a 96% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420563B2
Source datasetuspto-grants-2013_04
ORD IDord-a74df035e0e849d58d78327a2e94839a
Source noteuspto-grants-2013_04