HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477410Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 14855594, compound
https://huagongshe.com/reaction/477410
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,2-Difluoro-4-nitrobenzene | HCID 123053 | — |
| Reactant | HCID 86742213 | HCID 86742213 | — |
| Product | HCID 14855594 | HCID 14855594 | — |
Reaction Steps
To a stirred mixture of methyl 2-(2-fluoro-4-hydroxyphenoxy propanoate (4.0 g, 0.019 mole), potassium carbonate (2.9 g, 0.021 mole) and dimethyl sulfoxide (25 ml), was added 3,4-difluoronitrobenzene (3.0 g, 0.019 mole), all at once. The temperature was raised to 50° C., and held there for 19 hours. After this time, the resultant mixture was cooled to room temperature, then diethyl ether (50 ml) was added. This was filtered, and the filtrate was diluted with additional diethyl ether (150 ml). The latter solution was washed with 2N HCL (2×100 ml), then water (3×100 ml). After drying (MgSO4) and filtering, the diethyl ether was removed by distillation. A brown viscous oil resulted (6.2 grams, 92 percent). NMR spectroscopy (1H, 19F) confirmed the structure as consistent with the structure for the desired product. It was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04888050 |
|---|
| Source dataset | uspto-grants-1989_12 |
|---|
| ORD ID | ord-9610b0a11ac341c392ae97bf7f41caa2 |
|---|
| Source note | uspto-grants-1989_12 |
|---|