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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575970Generated: October 28, 2026

Iodine → HCID 67403681, compound

https://huagongshe.com/reaction/575970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Bromo-3,5-difluorobenzeneHCID 136313—
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67403681HCID 6740368130.7%

Reaction Steps

To a solution of 1-bromo-3,5-difluorobenzene (8 g, 41.4 mmol) in dry tetrahydrofuran (100 ml), under nitrogen, was added magnesium turnings (0.99 g, 41.4 mmol) and one crystal of iodine. The mixture was refluxed for 1 h, cooled to ambient temperature and a solution of 1-N-boc-3-pyrrolidone (7.66 g, 41.4 mmol) in dry tetrahydrofuran (40 ml) was added drop wise. The resulting mixture was refluxed 1 h, cooled to ambient temperature, aqueous saturated ammonium chloride solution (50 ml) was added and the mixture was extracted with ethylacetate (3×50 ml). The combined organic phase was washed with brine, dried (Na2SO4), filtered and evaporated to dryness. The crude product was purified by flash column chromatography (ethylacetate/isooctane, 1:9 to 1:1) to give the title compound (3.8 g, 30%). MS m/z (rel. intensity, 70 eV) 299 (M+, 1), 243 (30), 198 (39), 127 (36), 57 (bp).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035073B2
Source datasetuspto-grants-2015_05
ORD IDord-563bb46668884287b88dc248707fbe59
Source noteuspto-grants-2015_05