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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Methoxy-4-nitrobenzoic acid | HCID 78764 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-methoxy-4-nitro-benzoyl Chloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067506B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-6c3b7e4f21cb4ad4b499a22e39c76828 |
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| Source note | uspto-grants-2006_06 |
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