HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl (4-chlorophenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | (4-Chlorophenyl)acetic acid | HCID 15880 | — |
| Solvent | p-Toluenesulfonic acid | HCID 6101 | — |
| Product | Ethyl (4-chlorophenyl)acetate | HCID 84177 | — |
Reaction Steps
First, 17.24 g of 4-chlorophenylacetic acid was dissolved in 200 ml of ethanol, to which a catalytic amount of p-toluenesulfonic acid was added, and the mixture was heated under reflux for 10 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and concentrated. The residue was poured into water and extracted with ethyl acetate, and the organic layer was dried and then concentrated. The residue was subjected to silica gel chromatography, which afforded 19.0 g of ethyl 4-chlorophenylacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06100257 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-798996bbe3554d8bb59696b26da3d550 |
| Source note | uspto-grants-2000_08 |