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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Reactant6-Fluoro-3,4-dihydro-2H-1-benzopyran-2-carboxaldehydeHCID 11694000—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Product6-Fluoro-2-(oxiran-2-yl)chromanHCID 11658439—

Reaction Conditions

Temperature30 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633241B2
Source datasetuspto-grants-2014_01
ORD IDord-d3315c5fd4f94569b9b83e8c150e6028
Source noteuspto-grants-2014_01