Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Methoxy-2-nitroaniline | HCID 66793 | — |
| Reactant | Methyl [4-(chlorosulfonyl)-3,5-dimethylphenoxy]acetate | HCID 20786562 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20786539 | HCID 20786539 | — |
Reaction Steps
A mixture of methyl (4-chlorosulfonyl-3,5-dimethylphenoxy)acetate (Intermediate A1, 7.6 g, 0.026 mol), 4-methoxy-2-nitroaniline (4.0 g, 0.024 mol), and pyridine (50 mL) was stirred at room temperature for 16 hr, in a 90° C. bath for 5 hr, and in a 130° C. bath for 30 min. The mixture was cooled and stirred with toluene for 10 min. The resulting suspension was filtered, and the filtrate was concentrated, diluted with 150 mL toluene and 100 mL ethyl acetate, washed with 1 M hydrochloric acid and water, and concentrated to about 50 mL. The mixture was left overnight in a freezer. The solid was collected and washed with several portions of cold toluene. After drying, it weighed 8.2 g (74%). Another 0.45 g portion of the title compound was recovered from extraction of aqueous phases and crystallization of a second crop from the toluene filtrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06897227B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-43c026c1a2e54e3485b72943114f7568 |
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| Source note | uspto-grants-2005_05 |
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