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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750917Generated: November 3, 2026

Pyridine → N-(1,3-dibromodibenzo[b,d]furan-4-yl)acetamide

https://huagongshe.com/reaction/1750917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
Reactant1,3-Dibromodibenzo[b,d]furan-4-amineHCID 58401066—
SolventDichloromethaneHCID 6344—
ProductN-(1,3-dibromodibenzo[b,d]furan-4-yl)acetamideHCID 5840085770.3%

Reaction Steps

In a 2 L round-bottomed flask, 1,3-dibromodibenzo[b,d]furan-4-amine (76 g, 223 mmol) in dichloromethane (800 mL) and pyridine (180 mL, 2229 mmol) were cooled by ice bath. Acetyl chloride (31.7 mL, 446 mmol) was added dropwise while stirring. Then the ice bath was removed. The reaction was stirred at room temperature for 1 h. The residue was collected by filtration and washed by water and dichloromethane to give N-(1,3-dibromodibenzo[b,d]furan-4-yl)acetamide (60 g, 70.3% yield) as brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156870B2
Source datasetuspto-grants-2015_10
ORD IDord-61240f818c4c40c08651ddf6cc23109d
Source noteuspto-grants-2015_10