HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-(Chloromethyl)-2-hydroxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | 3-(Chloromethyl)benzaldehyde | HCID 22395331 | — |
| Product | 5-(Chloromethyl)-2-hydroxybenzaldehyde | HCID 335291 | — |
Reaction Steps
The salicylaldehyde is convened to the 5-chloromethylbenzaldehyde by combining the aldehyde with aqueous formaldehyde (37%) and concentrated hydrochloric acid, at a reduced temperature in the range of -10° to +10° C. or thereabouts. Gaseous HCl is then bubbled through the solution to saturate with HCl after which the solution is stirred for a period sufficient to effect the reaction at a reduced temperature, one which is about that of the temperature at which the reactants were combined initially. The product, the 5-(chloromethyl)-2-hydroxybenzaldehyde, should be formed as a white precipitate which can be recovered by conventional means.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05569677 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-7b2ae60820514fec831f7a77ccc9ca35 |
| Source note | uspto-grants-1996_10 |