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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750914Generated: October 26, 2026

Acetyl chloride → 2-Phenoxyacetanilide

https://huagongshe.com/reaction/1750914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantBenzenamine, 2-phenoxy-HCID 75899—
SolventDichloromethaneHCID 6344—
Product2-PhenoxyacetanilideHCID 89708098%

Reaction Conditions

Temperature0 °C

Reaction Steps

The mixture of 2-phenoxyaniline (100 g, 540 mmol), triethylamine (0.090 L, 648 mmol) and 1 L dichloromethane was cooled to 0° C. by ice bath. Acetyl chloride (0.04 L, 567 mmol) was added dropwise. After the addition completed, the reaction was stirred under room temperature for 2 h. The mixture was concentrated and diluted by dichloromethane. The organic phase was washed by water and dried over sodium sulfate. The crude product was purified by silica gel column (20% EtOAc in hexane) to give red brown oily solid N-(2-phenoxyphenyl)acetamide (120 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156870B2
Source datasetuspto-grants-2015_10
ORD IDord-1404d205651c425bac288e7484b73921
Source noteuspto-grants-2015_10