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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455701Generated: October 29, 2026

Iodine → 7-Bromo-1-fluoro-3-(neopentyloxy)spiro[chromeno[2,3-c]pyridine-5,2'-oxirane]

https://huagongshe.com/reaction/455701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant7-bromo-1-fluoro-5-methylene-3-(neopentyloxy)-5H-chromeno[2,3-c]pyridineHCID 67382956—
CatalystSilver(II) oxideHCID 92152—
SolventTetrahydrofuranHCID 8028—
Product7-Bromo-1-fluoro-3-(neopentyloxy)spiro[chromeno[2,3-c]pyridine-5,2'-oxirane]HCID 8676197396.4%

Reaction Steps

To a solution of 7-bromo-1-fluoro-5-methylene-3-(neopentyloxy)-5H-chromeno[2,3-c]pyridine (995 mg, 2.63 mmol) in THF (60 mL)/Water (10 mL) was added iodine (1335 mg, 5.26 mmol) and silver oxide (1219 mg, 5.26 mmol). The reaction mixture was allowed to stir at rt for 20 min. K2CO3 (545 mg, 3.95 mmol) was added in one portion and the reaction mixture was allowed to stir for 30 min. The reaction mixture was filtered through a pad of celite. The reaction mixture was partitioned between water and EtOAc. The organic phase was separated, dried over Na2SO4. The solvent was removed under reduced pressure to afford 7-bromo-1-fluoro-3-(neopentyloxy)spiro[chromeno[2,3-c]pyridine-5,2′-oxirane] as a yellow solid (1000 mg) which was taken onto the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497264B2
Source datasetuspto-grants-2013_07
ORD IDord-4a13aafc805946368c57a775fc5318ea
Source noteuspto-grants-2013_07