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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256405Generated: October 29, 2026

Iodine → HCID 10476981, compound

https://huagongshe.com/reaction/2256405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPyridineHCID 1049—
ReactantHCID 9977053HCID 9977053—
SolventChloroformHCID 6212—
ProductHCID 10476981HCID 10476981—

Reaction Steps

N-Allyl-N-carbobenzyloxy-4-(3-pyridyl)-3,5-difluoroaniline (PREPARATION 4, 496 mg 1.31 mmol) in chloroform (25 ml), pyridine (1.58 ml, 19.6 mmol, 15 eq) and iodine (4.97 g, 19.6 mmol, 15 eq) are combined. The resulting mixture is placed under an atmosphere of nitrogen and heated to 50° with stirring. After 1.5 hr, the reaction is decanted into chloroform (70 ml). The remaining sludge is rinsed with chloroform (3×15 ml). The combined organics are washed with sodium thiosulfate (20%), then brine, dried (sodium sulfate), filtered and concentrated under reduced pressure to give a solid. This material is purified by silica gel chromatography (100 g) eluting with methanol/chloroform (0.5/99.5-1 l, 1/99, 1 l). The appropriate fractions are pooled and concentrated to give the title compound, mp 133°-134°; FTIR (mull) cm-1 3130, 1758, 1650, 1414, 1241, 1017 and 846; NMR (CDCl3) 8.72, 8.62, 7.79, 7.43-7.38, 7.32, 4.84-4.72, 4.19, 3.80, 3.51 and 3.39 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654435
Source datasetuspto-grants-1997_08
ORD IDord-3783aec9fe17417cb2798233b59c6774
Source noteuspto-grants-1997_08