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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243211Generated: November 2, 2026

Water → (3-Bromophenyl)acetonitrile

https://huagongshe.com/reaction/2243211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant2-(3-bromophenyl)acetamideHCID 11736027—
Solvent1,4-DioxaneHCID 31275—
Product(3-Bromophenyl)acetonitrileHCID 36023—

Reaction Steps

2-(3-Bromophenyl)acetamide (10.0 g, 46.73 mmol) (example 1) in dry 1,4-dioxane (100 mL) was cooled to 0° C. Triethylamine (18.91 g, 187.92 mmol) was added and the reaction mixture was stirred for about 10 minutes. Trifluoroacetic anhydride (39.26 g, 186.92 mmol) was added dropwise at 0° C. and the reaction mixture was stirred at room temperature for about 12 hours. The reaction mixture was poured into cold water, extracted with ethyl acetate, washed with water, dried over anhydrous sodium sulphate, filtered and the solvent evaporated under vacuum. An oily residue was obtained which was purified by column chromatography over silica gel using ethyl acetate and hexane (1:49) to afford the title compound as light yellow colored oil. Yield: 8.4 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674811B2
Source datasetuspto-grants-2010_03
ORD IDord-7d933871668142a38797fe91a2d5d3aa
Source noteuspto-grants-2010_03