HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722683Generated: October 30, 2026
(3-Bromopropyl)benzene → HCID 54429308, compound
https://huagongshe.com/reaction/722683
Participants
| Role | Name | HCID | Charge |
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| Reactant | (3-Bromopropyl)benzene | HCID 12503 | — |
| Reactant | HCID 86608799 | HCID 86608799 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54429308 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07138413B1 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-d24b1f57e81f47d79478350280ecb3eb |
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| Source note | uspto-grants-2006_11 |
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