HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454508Generated: October 30, 2026
Potassium Iodide → Methyl 2-(benzyloxy)-5-(morpholin-4-yl)benzoate
https://huagongshe.com/reaction/454508
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Bis(2-chloroethyl) ether | HCID 8115 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 5-amino-2-(benzyloxy)benzoate | HCID 23019162 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Methyl 2-(benzyloxy)-5-(morpholin-4-yl)benzoate | HCID 66990981 | — |
Reaction Steps
Potassium carbonate (0.54 g), potassium iodide (0.11 g), and bis(2-chloroethyl)ether (0.22 mL) were sequentially added to an N,N-dimethylacetamide (3.2 mL) solution of methyl 5-amino-2-(benzyloxy)benzoate (0.40 g), followed by stirring at 100° C. for 3 hours. The reaction mixture was cooled to room temperature, and then water and ethyl acetate were added thereto. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 85-60% hexane/ethyl acetate] to obtain 0.27 g of methyl 2-(benzyloxy)-5-(morpholin-4-yl)benzoate as a light yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08492582B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-85dd3bddb98b49e18ad728a192720a65 |
|---|
| Source note | uspto-grants-2013_07 |
|---|