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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645490Generated: October 25, 2026

Acetoxyacetyl chloride → HCID 59824354, compound

https://huagongshe.com/reaction/1645490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoxyacetyl chlorideHCID 26297—
Reactant3-(Allyl-methyl-carbamoyl)-5-amino-2,4,6-triiodo-benzoyl chlorideHCID 59824364—
SolventDimethylacetamideHCID 31374—
ProductHCID 59824354HCID 5982435491%

Reaction Steps

3-(Allyl-methyl-carbamoyl)-5-amino-2,4,6-triiodo-benzoyl chloride (8) (5 g, 7.93 mmol) was dissolved in dry DMA (20 mL) was acetoxyacetyl chloride (1.7 mL, 15.9 mmol) was added dropwise. The reaction mixture was stirred at overnight at RT, with nitrogen bubbling through the reaction mixture. The reaction was monitored by TLC on silica gel plates eluting with ethyl acetate: petrol (1:1). (6) had an Rf of 0.62 and 0.76 whilst there were two new spots at 0.32 and 0.22. The solution was diluted with ethyl acetate (˜100 mL) and washed with ice water/brine (50:50, 20 ml×5). The organics were dried over MgSO4, filtered, concentrated and dried under high vacuum to give the desired compound (5.26 g, 91%). The structure was confirmed by 1H and 13C NMR, and purity by LCMS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124806B2
Source datasetuspto-grants-2012_02
ORD IDord-8d6405662a994c9d8c17afa5f36a0346
Source noteuspto-grants-2012_02