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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830728Generated: October 31, 2026

Thionyl Chloride → 3-methoxy-4-nitro-benzoyl Chloride

https://huagongshe.com/reaction/1830728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-Methoxy-4-nitrobenzoic acidHCID 78764—
Solvent1,4-DioxaneHCID 31275—
Product3-methoxy-4-nitro-benzoyl ChlorideHCID 11127655—

Reaction Steps

Thionyl chloride 3.7 mL, (50 mmol) was added drop wise, at room temperature, to a stirred solution of 3-methoxy-4-nitro-benzoic acid (1.0 g, 5.07 mmol) in 15 mL of dioxane under a nitrogen atmosphere. After the addition was complete, the reaction was allowed to stir at room temperature for 1 hr. The reaction flask was then fitted with a distillation head, and excess thionyl chloride and about ½ of the solvent was removed by distillation in a 120° C. oil bath. The remaining solvent was removed by rotary evaporation, and the residue was taken up in 20 mL toluene and again about 1 of the solvent was removed by distillation. The remaining solution was then cooled to 0° C., and the white solid which precipitated, was collected by suction filtration, and rinsed with 1-1 Et2O-hexane. 1H-NMR (400 MHz, CDCl3) δ7.87 (d, J=7.83 Hz, 1H), 7.82 (d, J=7.83 Hz, 1H), 7.77 (s, 1H), 4.04 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067506B2
Source datasetuspto-grants-2006_06
ORD IDord-6c3b7e4f21cb4ad4b499a22e39c76828
Source noteuspto-grants-2006_06