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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604390Generated: October 30, 2026

(3-Bromopropyl)benzene → HCID 54429308, compound

https://huagongshe.com/reaction/604390

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Bromopropyl)benzeneHCID 12503—
ReactantHCID 86608799HCID 86608799—
SolventTolueneHCID 1140—
ProductHCID 54429308HCID 54429308—

Reaction Steps

4-(Piperidinomethyl)benzoic acid methyl ester (22 mmol) in dry tetrahydrofurane was added dropwise to a suspension of 44 mmol of lithium aluminium hydride in 30 ml of dry tetrahydrofurane at 0° C. After refluxing for 2 hours a saturated solution of ammonium chloride in water was added dropwise. After stirring for 12 hours at ambient temperature the organic layer was isolated and the aqueous layer extracted with methylene chloride. The organic extracts were combined and the solvent was evaporated under reduced pressure. The residue was crystallized with maleic acid from diethyl ether/2-propanol (Yield: 91%). Sodium 4-(piperidinomethyl)benzyl alcoholate (5 mmol) and 6 mmol of 3-phenylpropyl bromide in 10 ml of dry toluene were refluxed for 6 hours. The solvent was evaporated under reduced pressure. The residue was purified by rotatory chromatography on silica gel using methylene chloride/ammonia atmosphere as eluent. The product was crystallized with oxalic acid from diethyl ether/ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910605B2
Source datasetuspto-grants-2011_03
ORD IDord-3221b2c63e824ce0a7cf35d82073681b
Source noteuspto-grants-2011_03