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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397402Generated: October 30, 2026

Methyl iodide → Methyl 5-cyano-2-methoxybenzoate

https://huagongshe.com/reaction/1397402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-cyano-2-hydroxybenzoateHCID 10583428—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-cyano-2-methoxybenzoateHCID 1846478928%

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of acid methyl 5-cyano-2-hydroxybenzoate (2 g, 11.2 mmol) in dry acetone (50 mL) was cooled to 0° C. and K2CO3 (2.34 g, 16.9 mmol) followed by MeI (1.1 mL, 16.9 mmol) were added dropwise. The reaction mixture was allowed to stir at 65° C. for 10 h and then diluted with EtOAc. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to yield methyl 5-cyano-2-methoxybenzoate (600 mg, crude), which was carried through without further purification. 1H NMR (300 MHz, CDCl3) δ 8.11 (d, J=2.2 Hz, 1H), 7.78-7.74 (dd, J=8.8 Hz, 2.2 Hz, 1H), 7.08-7.05 (d, J=8.8 Hz, 1H), 3.98 (s, 3H), 3.92 (s, 3H). MS (ESI) m/z: Calculated for C10H9NO3: 191.06. found: 191.8 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-6a3b89f87a904c3292c19142565c50f8
Source noteuspto-grants-2014_12