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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2446Generated: October 25, 2026

4-Nitrobenzoyl chloride → N-(1,3-benzodioxol-5-yl)-4-nitrobenzamide

https://huagongshe.com/reaction/2446

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
Reactant1,3-Benzodioxol-5-amineHCID 84310—
ProductN-(1,3-benzodioxol-5-yl)-4-nitrobenzamideHCID 67422187.2%

Reaction Steps

Using 3,4-methylenedioxyaniline (1.44 g, 10.5 mmol) and 4-nitrobenzoyl chloride (1.86 g, 10.0 mmol), the procedure of Reference Example 11 was repeated to obtain 2.49 g (87.2%) of the title compound in the form of yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728835
Source datasetuspto-grants-1998_03
ORD IDord-b04fe9c2f1da4526a30f3f2067ac49b1
Source noteuspto-grants-1998_03