Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Methyl-4-nitrobenzoic acid | HCID 18370 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | Methyl 3-methyl-4-nitrobenzoate | HCID 260927 | 95% |
Reaction Steps
To a stirred suspension of 3-methyl-4-nitrobenzoic acid (100 g, 0.55 mole) in methanol (400 mL) was added thionyl chloride (36 g, 0.30 mole), over a period of 1 hour (the temperature of the reaction mixture rising to about 35°-40° C.). The mixture was heated to reflux for 1.5 hours, then cooled to 50°-55° C. and maintained at this temperature for 30 minutes prior to cooling to ambient temperature. Water (100 mL) was added over 30 minutes, with cooling applied to maintain the temperature at 20°-25° C. Filtration was followed by washing of the solid with water (100 mL twice), and drying at 40° C. under vacuum, to afford 103 g (95%) of methyl 3-methyl-4-nitrobenzoate as a yellow solid; mp 83°-85° C.; NMR (250 MHz, CDCl3): 2.62 (s, 3H, ARCH3) , 3.98 (s, 3H, CO2CH3), 8.01 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05334765 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-c57ac6f021a845c1b94d865413d34ab1 |
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| Source note | uspto-grants-1994_08 |
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