Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089260Generated: October 26, 2026

Iodine → 5-Iodo-6-methyl-2-oxo-1-(3-(trifluoromethyl)phenyl)-1,2-dihydropyridine-3-carboxylic acid

https://huagongshe.com/reaction/2089260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
Reactant6-Methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxylic acidHCID 11702104—
SolventAcetic AcidHCID 176—
Product5-Iodo-6-methyl-2-oxo-1-(3-(trifluoromethyl)phenyl)-1,2-dihydropyridine-3-carboxylic acidHCID 5821804685.7%

Reaction Steps

To acetic acid (263.7 L, 6.8 rel vol) was charged 6-methyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxylic acid (38.6 kg, 1 mol eq, limiting reagent), iodine (17.4 kg, 0.53 mol eq) and concentrated sulfuric acid (3.7 L, 0.1 rel vol). The temperature was adjusted to 50° C.-55° C. and 90% nitric acid (4.1 kg, 0.6 mol eq) charged over 15 minutes. The reaction was stirred until deemed to be complete as judged by HPLC analysis. The reaction was cooled, stirred and the product collected by filtration. The solid was washed twice with water (2×77.0 L, 2×2 rel vol) and acetone (2×38.6 kg, 2×1 rel vol). The solid was dried under vacuum to constant weight to yield the title compound (47.0 kg, 111.0 mol, 85.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436024B2
Source datasetuspto-grants-2013_05
ORD IDord-3b1623ffc1794b06a4315aceb2e681b2
Source noteuspto-grants-2013_05