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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398370Generated: November 1, 2026

Sodium Iodide → Methyl 4-iodo-2-methylnicotinate

https://huagongshe.com/reaction/1398370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetyl chlorideHCID 6367—
ReactantMethyl 4-chloro-2-methylpyridine-3-carboxylateHCID 84070460—
SolventAcetonitrileHCID 6342—
ProductMethyl 4-iodo-2-methylnicotinateHCID 8671036222.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 4-chloro-2-methylnicotinate (6.00 g, 32.3 mmol) in acetonitrile (80 mL) was added acetyl chloride (3.45 mL, 48.5 mmol) followed by sodium iodide (48.5 g, 323 mmol). The reaction mixture was heated at 80° C. for 16 hrs. The reaction mixture was evaporated to dryness and the residue was adjusted to pH 6 by adding saturated potassium carbonate solution. The product was extracted with dichloromethane (250 mL). The organic phase was washed with brine (2×100 mL), dried over Na2SO4, and concentrated under reduced pressure to afford methyl 4-iodo-2-methylnicotinate (2.00 g, 7.22 mmol, 22% crude yield) as colorless semisolid which was carried on without further purifications. LC/MS (ESI) m/e 278.0 [(M+H)+, calcd for C8H9INO2 278.0]; LC/MS retention time (method C): tR=2.13 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901305B2
Source datasetuspto-grants-2014_12
ORD IDord-07bf48f296c6406891da134616c43eec
Source noteuspto-grants-2014_12