HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-Hydroxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Product | Salicylaldehyde | HCID 6998 | — |
Reaction Steps
Sen et al J. Indian Chem. Soc. 9 173 (1932) state that the use of chloroform in an ethyl alcohol solution in the Reimer-Tiemann reaction increases the yield of aldehyde. However, the only example describing the reaction of phenol with chloroform and sodium hydroxide in aqueous ethyl alcohol shows a combined yield for salicylaldehyde and p-hydroxybenzaldehyde of only 33%, based on the phenol reacted. The proportion of salicylaldehyde to p-hydroxybenzaldehyde in the product is about five to one, the same as for the conventional aqueous reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04351962 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-7fc6fb7987b64c39b04f5870873d42c4 |
| Source note | uspto-grants-1982_09 |