HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloroethyl 5-(2,4-difluorophenyl)salicylate → 1-(Ethoxycarbonyloxy)ethyl 5-(2,4-difluorophenyl)salicylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloroethyl 5-(2,4-difluorophenyl)salicylate | HCID 20266758 | — |
| Reactant | Sodium ethyl carbonate | HCID 23677505 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(Ethoxycarbonyloxy)ethyl 5-(2,4-difluorophenyl)salicylate | HCID 13491395 | — |
Reaction Steps
To a solution of 1-chloroethyl 5-(2,4-difluorophenyl)salicylate (5.0 g) in about 40 ml of DMF is added portionwise 3.0 g of sodium ethyl carbonate. The reaction is stirred at room temperature and then concentrated in vacuo. The concentrate is partitioned between ether/ethyl acetate and acidified water. The organic layer is separated and the aqueous layer is again extracted with ether, the organic layers are pooled and washed with water followed by drying and concentration to the crude product. After further purification by chromatography as described in Example 1, the product is crystallized from hexane to afford pure 1-(ethoxycarbonyloxy)ethyl 5-(2,4-difluorophenyl)salicylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04542158 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-2e181670a9584618adce48a18302962e |
| Source note | uspto-grants-1985_09 |