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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927716Generated: November 1, 2026

4-Aminophenol → 3,4-dichloro-N-(4-hydroxyphenyl)benzamide

https://huagongshe.com/reaction/1927716

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantPyridineHCID 1049—
ReactantBenzoyl chloride, 3,4-dichloro-HCID 76403—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3,4-dichloro-N-(4-hydroxyphenyl)benzamideHCID 97680838%

Reaction Steps

4-Aminophenol (1.9 g, 17 mmol) was diluted with DMF (40 mL) followed by the addition of pyridine (0.978) (1.4 mL, 17 mmol) and 3,4-dichlorobenzoyl chloride (3.0 g, 14 mmol) in 5 mL of DMF. After stirring for 12 hours, the reaction mixture was diluted with ethyl acetate and 2N HCl. The aqueous layer was extracted once with ethyl acetate. The organics were combined, washed with water, brine, dried over MgSO4, filtered and concentrated onto silica gel. The material was purified using a biotage 40M column eluting with hexanes:ethyl acetate (9:1) using 2 L and then (60:40) 1 L to yield 3,4-dichloro-N-(4-hydroxyphenyl)-benzamide (1.5 g, 37% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183289B2
Source datasetuspto-grants-2012_05
ORD IDord-39d3dff4032a4ed8ad3f3ff6d887d579
Source noteuspto-grants-2012_05