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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1408286Erstellt: 26. Oktober 2026

Boric Acid → 5-(N-allylacetamido)-N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide

https://huagongshe.com/reaction/1408286

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoric AcidHCID 7628—
EduktAllyl bromideHCID 7841—
EduktPotassium HydroxideHCID 14797—
Edukt5-Acetamido-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamideHCID 11115326—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt5-(N-allylacetamido)-N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamideHCID 59622893—

Reaktionsschritte

To a stirred solution of 5-acetamido-N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide (7.5 g, 10 mmol) and boric acid (1.24 g, 20 mmol) in water (10 ml) and methanol (7 ml) is added potassium hydroxide (10 M) drop wise until a stable pH 12.5 is established. Allylbromide (860 ul, 10 mmol) is added and potassium hydroxide (10 M) is continuously added to maintain pH 12.5. for 3 h and the mixture is then left stirring over night. The following day the mixture is reduced in vacuo to remove methanol, the resulting aqueous phase is diluted with 50 ml water and treated with acidic and basic ion exchanger. Resins are removed and rinsed and the combined aqueous volume is reduced to dryness in vacuo to yield 5-(N-allylacetamido)-N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08920780B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-9817ee3996d447b9978d3ebc43a01a3e
Quellennotizuspto-grants-2014_12