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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471348Generated: October 30, 2026

Methanol → Methyl 2-bromo-4-methoxybenzoate

https://huagongshe.com/reaction/1471348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Bromo-4-methoxybenzoic acidHCID 14484713—
SolventWaterHCID 962—
ProductMethyl 2-bromo-4-methoxybenzoateHCID 1511099785%

Reaction Conditions

Temperature79 °C

Reaction Steps

SOCl2 (7.5 mL, 103.0 mmol) is added dropwise to a stirred 0° C. suspension of 2-bromo-4-methoxybenzoic acid (3) (6.5 g, 28.1 mmol) in methanol (12 mL). The mixture is next stirred at 79° C. for 18 h and then cooled to room temperature before removal of methanol and excess SOCl2 at reduced pressure. The residue is diluted with H2O (50 mL) and extracted with ethyl acetate (100 mL and 70 mL). The extract is washed (2 N NaOH and brine) and dried. After solvent removal at reduced pressure, the residue is purified on silica gel (14.3% to 16.7% ethyl acetate/hexane) to give 5.9 g (85%) of 4 as a colorless liquid. IR 2952, 1728, 1597, 1261 cm−1; 1H NMR (CDCl3) δ 3.83 (s, 3H, CH3O), 3.89 (s, 3H, CO2CH3), 6.86 (dd, J=7.2, 2.0 Hz, 1H, 5-PhH), 7.18 (d, J=2.0 Hz, 1H, 3-PhH), 7.85 ppm (d, J=7.2 Hz, 1H, 6-PhH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012217B2
Source datasetuspto-grants-2015_04
ORD IDord-764c725f7f144c22ad483420dd343eec
Source noteuspto-grants-2015_04