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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280236Generated: October 30, 2026

Acetonitrile → HCID 57384643, compound

https://huagongshe.com/reaction/2280236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPeracetic AcidHCID 6585—
ReactantIodide IonHCID 30165—
ReactantAmmonium AcetateHCID 517165—
ReactantSodiumHCID 5360545—
ReactantHCID 67973124HCID 67973124—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
ProductHCID 57384643HCID 57384643—

Reaction Steps

To sodium [123I] iodide, received in 5-20 μL 0.05M sodium hydroxide is added ammonium acetate buffer (100 μL pH 4.0, 0.2M), sodium [127I] iodide (10 μL, 1 mM solution in 0.01M sodium hydroxide, 1×10−8 moles), peracetic acid (PAA) solution (10 μL 1 mM solution, 1×10−8 moles) and finally 10-(5-tributylstannyl-isoxazol-3-yl)-decanoic acid solution in ethanol or acetonitrile (53 μg, 1×10−7 moles). The reaction mixture is allowed to stand at room temperature for 15 minutes and the iodinated product 10-(4-iodo-[1,2,3]triazol-1-yl)-decanoic acid purified by HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09138493B2
Source datasetuspto-grants-2015_09
ORD IDord-3e1936dbf9bd4930a437b7a446273b7e
Source noteuspto-grants-2015_09