HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 136388724, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-Iodoaniline | HCID 10893 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-tert-Butyl-2-hydroxybenzaldehyde | HCID 3678675 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 136388724 | HCID 136388724 | 96% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420563B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-a74df035e0e849d58d78327a2e94839a |
| Source note | uspto-grants-2013_04 |