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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantSodium HydroxideHCID 14798—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Methoxy-5-(4-nitrophenoxy)benzoic acidHCID 23023063—
SolventDichloromethaneHCID 6344—
Product4-(3-(N-methylcarbamoyl)-4-methoxyphenoxy)-1-nitrobenzeneHCID 2060913995%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841330B2
Source datasetuspto-grants-2014_09
ORD IDord-64566831b3e948519452b0238460a809
Source noteuspto-grants-2014_09