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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455591Generated: October 30, 2026

Iodine → 7-Bromo-3-chloro-1-fluorospiro[chromeno[2,3-c]pyridine-5,2'-oxirane]

https://huagongshe.com/reaction/455591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant7-bromo-3-chloro-1-fluoro-5-methylene-5H-chromeno[2,3-c]pyridineHCID 86640733—
CatalystSilver(II) oxideHCID 92152—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product7-Bromo-3-chloro-1-fluorospiro[chromeno[2,3-c]pyridine-5,2'-oxirane]HCID 8665836868.1%

Reaction Steps

To a solution of 7-bromo-3-chloro-1-fluoro-5-methylene-5H-chromeno[2,3-c]pyridine (33 g, 101 mmol) in THF (450 mL) were added successively water (69.2 mL), iodine (51.3 g, 202 mmol) and silver(II) oxide (46.8 g, 202 mmol) at RT. The reaction mixture was stirred at RT for 10 minutes before adding K2CO3 (41.9 g, 303 mmol). After 30 minutes, the reaction mixture was diluted with EtOAc and filtered through a pad of celite. The filter cake was washed with additional EtOAc. The combined filtrate was concentrated under reduced pressure upon which a white solid precipitated. The solid was filtered off. The filtrate was further concentrated under reduced pressure to obtain a residue which was triturated with ether to afford a white precipitate. The solid was filtered off, combined with the first solid and dried under reduced pressure to afford 7-bromo-3-chloro-1-fluorospiro[chromeno[2,3-c]pyridine-5,2′-oxirane] (23.56 g, 68.8 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497264B2
Source datasetuspto-grants-2013_07
ORD IDord-d58e5f760c21424cb577d8cd7a245300
Source noteuspto-grants-2013_07