HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045544Generated: October 25, 2026
Dimethyl Sulfoxide → 2-(3-Fluoro-4-methoxyphenyl)oxirane
https://huagongshe.com/reaction/1045544
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Fluoro-p-anisaldehyde | HCID 67696 | — |
| Reactant | Trimethylsulfonium iodide | HCID 75127 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-Fluoro-4-methoxyphenyl)oxirane | HCID 24699079 | — |
Reaction Steps
The title compound was prepared by following general procedure 3. DMSO was added to NaH (1 equiv.) and heated to 65° C. for 1 h. THF was added at the same temperature and heated for another 10 min. After 10 min., the reaction mixture was cooled to 0° C. Trimethylsulfonium iodide (1 equiv.) was added and stirred for 10 min. after which the solution of 3-fluoro-4-methoxybenzaldehyde (1 equiv.) in THF was added dropwise. After complete addition, the reaction mixture was stirred at RT for 2 h. The product was detected by LCMS and the reaction mixture was poured into ice water, extracted in diethyl ether (4×50 mL), dried over Na2SO4 and concentrated at 25° C. to obtain the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08569287B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-535dc651e2d74a28956c5af740e3bd2d |
|---|
| Source note | uspto-grants-2013_10 |
|---|