HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → HCID 18925383, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, 5-(bromomethyl)-1,3-bis(1,1-dimethylethyl)-2-methoxy- | HCID 12142455 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 18925383 | HCID 18925383 | 81.8% |
Reaction Steps
Under a nitrogen atmosphere 1,3-di (t-butyl)-2-methoxy-5-bromomethylbenzene (6.26 g, 20 mmol) is then reacted with 4-hydroxybenzaldehyde (2.44 g, 20 mmol) and potassium carbonate (3.04 g) in 140 ml of methyl ethyl ketone. The reaction mixture is heated to reflux and maintained at this temperature for about 18 hours at which time the reaction mixture is cooled. The inorganics are removed by filtration and the filtrate is concentrated in vacuo. The concentrated reaction products are purified by silica gel chromatography to yield 5.8 grams (81%) of 4-[[3,5-di (t-butyl)-4-methoxyphenyl]methoxy]benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251928B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-a6b6e34030cb4d149aafdeeb253b357d |
| Source note | uspto-grants-2001_06 |