HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-(2,2-Dichlorovinyloxy)-benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | 1-(Bromomethyl)-3-[(2,2-dichloroethenyl)oxy]benzene | HCID 20482706 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(2,2-Dichlorovinyloxy)-benzaldehyde | HCID 13489976 | — |
Reaction Steps
To a solution of 8.5 g of 3-(2,2-dichlorovinyloxy)-benzyl bromide in 12.6 ml of acetic acid and 12.6 ml of water are added 8.4 g of hexamethylene tetramine. The resultant solution is refluxed for two hours. Subsequently 10 ml of HC1 are added and the reaction mixture is stirred for half an hour at 100°-110° C. The solution is washed with 100 ml of water and extracted cold (3 times) with 100 ml of ethyl acetate. The extract is washed with sodium carbonate solution and evaporated, to yield 5.8 g of 3-(2,2-dichlorovinyloxy)-benzaldehyde as a yellowish-brown oil, which can be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04291056 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-7fe54801ba4f4bdbbb6f73b7ff4eab5f |
| Source note | uspto-grants-1981_09 |