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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852592Generated: October 30, 2026

Iodine → Methyl 3-iodo-4-methoxy-5-nitrobenzoate

https://huagongshe.com/reaction/852592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTert-Butyl nitriteHCID 10906—
ReactantMethyl 3-amino-4-(methyloxy)-5-nitrobenzoateHCID 63022111—
SolventTolueneHCID 1140—
ProductMethyl 3-iodo-4-methoxy-5-nitrobenzoateHCID 6935609196.6%

Reaction Steps

To a solution of methyl 3-amino-4-(methyloxy)-5-nitrobenzoate (D163) (370 mg, 1.64 mmol, 1 equiv) in toluene (20 ml) at 0° C. was added iodine (218 mg, 0.86 mmol, 0.5 equiv) then 1,1-dimethylethyl nitrite (200 mg, 1.75 mmol, 1.1 equiv) and the resulting mixture was stirred at room temperature for 15 h then partitioned between AcOEt and brine. The two layers were separated and the organic phase was dried over MgSO4 and concentrated in vacuo. Purification of the residue by flash chromatography on silica gel gave methyl 3-iodo-4-(methyloxy)-5-nitrobenzoate (D165) (280 mg, 51%) as a light brown solid. No molecular ion. RT=3.33 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-088853114f4744539a6364506dfee43c
Source noteuspto-grants-2007_08