HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473063Generated: October 30, 2026
Sulfoxonium, trimethyl-, iodide (1:1) → 6-Fluoro-2-(oxiran-2-yl)chroman
https://huagongshe.com/reaction/473063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | 6-Fluoro-3,4-dihydro-2H-1-benzopyran-2-carboxaldehyde | HCID 11694000 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 6-Fluoro-2-(oxiran-2-yl)chroman | HCID 11658439 | — |
Reaction Steps
To 234 ml of dimethyl sulfoxide was added 32 g of trimethyl sulfoxonium iodide. To it, potassium tertiary butoxide (16 g) was added and stirred for 1 h at 20-40° C. The reaction mixture was cooled and to it was added a solution of the compound obtained in Example 2 in dimethyl sulfoxide (26 ml.) while maintaining the temperature between 20°-40° C. for 1.5 hr. The reaction mixture was quenched in cold water. The aqueous layer was extracted with ethyl acetate, washed with water, concentrated under reduced pressure followed by product distillation to give 19.6 g of 6-fluoro-3,4-dihydro-2-oxiranyl-2H-1-benzopyran (VII) in the form of a mixture of A and B as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633241B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-d3315c5fd4f94569b9b83e8c150e6028 |
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| Source note | uspto-grants-2014_01 |
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