HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 2-[4-(4-chlorophenyl)benzyloxy]-2-phenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-[4-(4-Chlorophenyl)benzyloxy]-2-phenylacetic acid | HCID 9863351 | — |
| Product | Ethyl 2-[4-(4-chlorophenyl)benzyloxy]-2-phenylacetate | HCID 20555293 | — |
Reaction Steps
A solution of 2-[4-(4-chlorophenyl)benzyloxy]-2-phenylacetic acid (8.0 g.) in ethanol (200 ml.) containing concentrated sulphuric acid (1 ml.) was heated under reflux for 90 minutes, then cooled to room temperature, and carefully neutralised by addition of an excess of saturated aqueous bicarbonate solution. The mixture obtained was evaporated and the residue extracted thoroughly with ethyl acetate. The combined extracts were washed with water, dried (MgSO4) and evaporated to give ethyl 2-[4-(4-chlorophenyl)benzyloxy]-2-phenylacetate (6.65 g.), m.p. 50°-51° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04310544 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-849d0e41554c4a528911e78e602a55cf |
| Source note | uspto-grants-1982_01 |