HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495703Generated: November 1, 2026
Water → Methyl 3-[4-[2-(phenoxazin-10-yl)ethoxy]phenyl]-2-ethoxypropanoate
https://huagongshe.com/reaction/495703
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Phenoxazin-10-yl)ethyl methanesulfonate | HCID 11220463 | — |
| Reactant | 2-Ethoxy-3-(4-hydroxy-phenyl)-propionic acid methyl ester | HCID 14923994 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-[4-[2-(phenoxazin-10-yl)ethoxy]phenyl]-2-ethoxypropanoate | HCID 9824188 | 390.1% |
Reaction Steps
A mixture of 2-(phenoxazin-10-yl)ethyl methanesulfonate (1.75 g, 5.0 mmol), methyl 3-(4-hydroxyphenyl)-2-ethoxypropanoate (1.5 g, 0.68 mmol) and potassium carbonate (3.16 g) in dry dimethylformamide (20 mL) was stirred for 12 h at 80° C. The reaction mixture was cooled to room temperature (ca. 25° C.). Water (30 mL) was added and extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with water (50 mL), dried (Na2SO4) and evaporated. The residue was chromatographed using a mixture of ethyl acetate and pet. ether (1:9) to afford the title compound (1.15 g, 47%) as a white solid. mp 89-90° C. 1H NMR data matches with the desired product (see above).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06939988B1 |
|---|
| Source dataset | uspto-grants-2005_09 |
|---|
| ORD ID | ord-d5bfc8d7fc5b4b3383f3f72465e30523 |
|---|
| Source note | uspto-grants-2005_09 |
|---|