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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108377Generated: October 30, 2026

Benzyl Bromide → HCID 10589829, compound

https://huagongshe.com/reaction/1108377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHexamethylphosphoramideHCID 12679—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-Piperidinone, 3-methyl-1-(phenylmethyl)-HCID 11106446—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10589829HCID 10589829166.6%

Reaction Steps

The reaction of 3-methyl-1-phenylmethyl-2-piperidinone (3.65 g, 18 mmol) with benzyl bromide (4.84 g, 28.3 mmol) in the presence of lithium diisopropylamide (prepared by treating diisopropylamine (2.73 g, 27 mmol) with butyllithium in hexanes (2.5 M, 10.3 mL, 25.7 mmol)) in THF (45 mL) and HMPA (2.7 mL, 15.5 mmol) as described above in the preparation of Example 10, gave 8.80 g of pale yellow colored oil. Column chromatography over silica gel (hexanes-EtOAc, 9:1) afforded the product lactam (3.72 g, 71%) as a colorless viscous residue. Analytical sample was prepared by bulb-to-bulb distillation (pot temp. 150-155° C. (1.3 mmHg)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066666
Source datasetuspto-grants-2000_05
ORD IDord-a0cbb4ec79f241dbbeeb416f39b78069
Source noteuspto-grants-2000_05