HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylic Acid → 1-(Ethoxycarbonyloxy)ethyl salicylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylic Acid | HCID 338 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Carbonic acid, 1-chloroethyl ethyl ester | HCID 162095 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(Ethoxycarbonyloxy)ethyl salicylate | HCID 53826080 | — |
Reaction Steps
A mixture of 2.76 g salicylic acid, 2.02 g triethylamine and 3.5 gm 1-chloroethyl ethyl carbonate in 25 ml of toluene is refluxed for three hours. The reaction mixture is cooled and 25 ml of ether and 25 ml of water added. The organic layer is separated, washed 2× with 25 ml water, dried through sodium sulfate and concentrated in vacuo. The residue (3.88 g) is chromatographed on 200 g silica gel. Elution with 25% methylene chloride in hexane gives 1-(ethoxycarbonyloxy)ethyl salicylate which is directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04542158 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-a70b2a22e28b40d7b4e2dc80c76ead48 |
| Source note | uspto-grants-1985_09 |