HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384785Generated: October 30, 2026
Acetic Acid → Methyl 5-methoxy-4-(4-chlorobutoxy)-2-nitrobenzoate
https://huagongshe.com/reaction/384785
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | HCID 10192903 | HCID 10192903 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 5-methoxy-4-(4-chlorobutoxy)-2-nitrobenzoate | HCID 10215101 | 934.8% |
Reaction Steps
In a 50 mL volume glass flask equipped with a stirrer, a thermometer and a dropping funnel were placed 10.1 g (36.7 mmol) of methyl 4-(4-chlorobutoxy)-3-methoxybenzoate (purity: 98%) obtained in Example II-18, 0.25 g (3.67 mmol) of sodium nitrite, and 12.5 mL of acetic acid. The resulting mixture was heated to 40° C. under stirring. To the reaction mixture was dropwise added slowly 115.4 g (146.8 mmol) of nitric acid (60 wt. %), and the mixture was heated at 40-50° C. for 5 hours. After the reaction was complete, 20 mL of water was added to the reaction mixture, and the aqueous mixture was cooled to 20° C., precipitating a crystalline product. The crystalline product was collected by filtration, washed successively with 30 mL of water and 30 mL of n-heptane, and dried under reduced pressure, to give 10.9 g (isolated yield: 92.0%, purity: 99% in terms of area percentage determined by high performance liquid chromatography) of methyl 5-methoxy-4-(4-chlorobutoxy)-2-nitrobenzoate as a white crystalline product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367824B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-d651b0245f8a4e25b38b89608b9c2227 |
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| Source note | uspto-grants-2013_02 |
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