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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34971Generated: October 25, 2026

5-Bromopentanenitrile → 4-(2-Propyl-3-chlorophenoxy)butane nitrile

https://huagongshe.com/reaction/34971

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-BromopentanenitrileHCID 79435—
Reactant2-Propyl3-chlorophenolHCID 15747295—
Product4-(2-Propyl-3-chlorophenoxy)butane nitrileHCID 21297257—

Reaction Steps

Five and seven-tenths grams of 2-propyl3-chlorophenol were then reacted with 5.9 ml. of 5bromovaleronitrile following the procedure of Example 2A. The resulting 4-(2-propyl-3-chlorophenoxy)butane nitrile was provided by chromatography. This purified nitrile intermediate (3.3 g.) was dissolved in about 65 ml. of methylene chloride to which 3.0 g. of aluminum chloride and 1.7 ml. of acetyl chloride had been added and the reaction was heated to reflux overnight. The reaction was cooled, additional methylene chloride was added, and the mixture was poured into ice/hydrochloric acid. The layers were separated and the organic layer was washed first with an aqueous sodium bicarbonate solution and then with water. The organic solution was dried over sodium sulfate and evaporated to dryness. Purification by chromatography provided 2.67 g. of the desired 4-(2-propyl-3-chloro4-acetylphenoxy)butane nitrile. NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764521
Source datasetuspto-grants-1988_08
ORD IDord-f52101a2e8e040ccb3b160f565907bd0
Source noteuspto-grants-1988_08