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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671013Generated: October 30, 2026

Water → Methyl 2-methoxy-3-nitrobenzoate

https://huagongshe.com/reaction/1671013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-hydroxy-3-nitrobenzoateHCID 596904—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-methoxy-3-nitrobenzoateHCID 59080598.9%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of methyl 2-hydroxy-3-nitrobenzoate (26.8 g, 136 mmol) in DMF (200 mL) was added K2CO3 (61 g, 440 mmol). Then iodomethane (62 g, 436 mmol) was added dropwise to the mixture at rt. The mixture was stirred at 45° C. for 5 h. Then the mixture was cooled to rt and water was added. The reaction mixture was extracted with EtOAc (500 mL×2). The combined organic layers were washed with water successively, dried over Na2SO4, filtered and concentrated under reduced pressure to give the title compound of Step B (28.4 g, 98.8% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 8.10 (dd, J=1.8 Hz, 8.4 Hz, 1H), 8.00 (dd, J=1.3 Hz, 8.2 Hz, 1H), 7.40 (dd, J=8.2 Hz, 8.4 Hz, 1H), 3.87 (s, 3H), 3.85 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994185B2
Source datasetuspto-grants-2011_08
ORD IDord-348fc5599d274c1daf7d8edcd1ea2c6b
Source noteuspto-grants-2011_08