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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254891Generated: October 31, 2026

Iodine → HCID 20094262, compound

https://huagongshe.com/reaction/2254891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantBis(trifluoroacetoxy)iodobenzeneHCID 102317—
ReactantHCID 11789375HCID 11789375—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 20094262HCID 2009426240.2%

Reaction Steps

(EXAMPLE 7B): 4-Amino-2,6-diethylpyridine (1.8 g) was added to a solution of iodine (3.1 g) and [bis(trifluoroacetoxy)iodo]benzene (5.7 g) in a mixture of dichloromethane (70 ml) and methanol (20 ml) and the mixture was stirred for 16 hours. Solvent was removed by evaporation and the residue was partitioned between ethyl acetate and a mixture of saturated sodium metabisulphite solution (50 ml) and saturated sodium carbonate solution (150 ml). The organic phase was separated, washed with saturated sodium chloride solution and dried. Solvent was removed by evaporation and the residue was purified by flash chromatography eluting with dichloromethane/methanol (97:3 v/v) to give 4-amino-2,6-diethyl-3-iodopyridine (1.33 g) as a solid, m.p. 72°-74° C.; NMR (CDCl3): 1.25(m,6H), 2.65(q,2H), 2.96(q,2H), 4.59(broad s,2H), 6.30(s,1H); mass spectrum (chemical ionisation, ammonia): 277(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05236937
Source datasetuspto-grants-1993_08
ORD IDord-0f4e7ade46c74d11a65433cf6a6e4667
Source noteuspto-grants-1993_08