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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400153Generated: November 2, 2026

Butyl bromide → HCID 67154048, compound

https://huagongshe.com/reaction/1400153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl bromideHCID 8002—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 4-nitrophenylacetateHCID 79517—
SolventDimethylformamideHCID 6228—
ProductHCID 67154048HCID 67154048—

Reaction Steps

10.46 g of ethyl 4-nitrophenylacetate are dissolved in 30 ml of DMF, added dropwise to a suspension of 2.0 g of sodium hydride in 20 ml of DMF with ice-cooling and stirred for 30 min. 5.394 ml of 1-bromobutane in 20 ml of DMF are subsequently added, and the mixture is stirred at 23° C. for 12 h. The reaction mixture is subsequently stirred into 100 ml of saturated ammonium chloride solution. The mixture is washed 4 times with 100 ml of ethyl acetate each time, the combined organic phases with 100 ml of sodium chloride solution, dried over sodium sulfate and, after filtration, evaporated to dryness in vacuo. The residue is purified by column chromatography (reversed phase). Yield: 11 g (83%) of ethyl 2-(4-nitrophenyl)hexanoate; LC-MS retention time: 2.44 min (“nonpolar” gradient).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906930B2
Source datasetuspto-grants-2014_12
ORD IDord-77dc743c028a40e3b84a7afe4dbdb1b0
Source noteuspto-grants-2014_12