HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78308Generated: October 29, 2026
Methylamine → 4-(3-(N-methylcarbamoyl)-4-methoxyphenoxy)-1-nitrobenzene
https://huagongshe.com/reaction/78308
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Methoxy-5-(4-nitrophenoxy)benzoic acid | HCID 23023063 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(3-(N-methylcarbamoyl)-4-methoxyphenoxy)-1-nitrobenzene | HCID 20609139 | 95% |
Reaction Steps
To a solution of 4-(3-carboxy-4-methoxyphenoxy)-1-nitrobenzene (0.50 g, 1.75 mmol) in CH2Cl2 (12 mL) was added SOCl2 (0.64 mL, 8.77 mmol) in portions. The resulting solution was heated at the reflux temp. for 18 h, cooled to room temp., and concentrated under reduced pressure. The resulting yellow solids were dissolved in CH2Cl2 (3 mL) then the resulting solution was treated with a methylamine solution (2.0 M in THF, 3.5 mL, 7.02 mmol) in portions (CAUTION: gas evolution), and stirred at room temp. for 4 h. The resulting mixture was treated with a 1N NaOH solution, then extracted with CH2Cl2 (25 mL). The organic layer was dried (Na2SO4) and concentrated under reduced pressure to give 4-(3-(N-methylcarbamoyl)-4-methoxyphenoxy)-1-nitrobenzene as a yellow solid (0.50 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841330B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-64566831b3e948519452b0238460a809 |
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| Source note | uspto-grants-2014_09 |
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