HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → HCID 18459584, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | p-Formylphenyl methacrylate | HCID 118924 | — |
| Reactant | HCID 178418435 | HCID 178418435 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18459584 | HCID 18459584 | — |
Reaction Steps
To the entire amount of the compound obtained in (3-1), 300 ml of THF and 100 ml of water were added and stirred. To this solution, sodium boron hydride was added little by little under ice cooling. Every each addition, disappearance of starting materials was confirmed by TLC. After the starting materials disappeared, water and ethyl acetate were added to the reaction solution and the reaction solution was extracted by liquid separation. The organic phase was dried over magnesium sulfate, concentrated and then subjected to silica gel column chromatography to produce the objective compound. The objective compound was obtained as a slightly brown oily product. Yield: 40.1 g (41.7%) (through two steps from 4-hydroxybenzaldehyde).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06432615B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-d5ac8cb13cc14ffeb8aae0c0f8ac937c |
| Source note | uspto-grants-2002_08 |