HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-tert-Butyl-2-hydroxybenzaldehyde → HCID 136388725, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-tert-Butyl-2-hydroxybenzaldehyde | HCID 3678675 | — |
| Reactant | 4-Ethynylaniline | HCID 3760025 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136388725 | HCID 136388725 | 43% |
Reaction Steps
3-tert-butyl salicylaldehyde (1) (0.70 g/3.93 mmol) and 4-ethynyl aniline (0.49 g/4.2 mmol) were dissolved in 100 ml of ethanol. Molecular sieves (3 Å, 15 g) and a few drops of glacial acetic acid were added and the mixture was stirred at room temperature for three days. After filtration over sodium sulphate and removal of the solvent, the residue was extracted several times with n-pentane. The solution was filtered again over sodium sulphate, and the solvent was removed. The title compound was obtained as a yellow powder. Yield: 43%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420563B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-21b81e8879ad45e68b356821b081f1c5 |
| Source note | uspto-grants-2013_04 |