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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552339Generated: October 29, 2026

Hydrochloric Acid → HCID 67164696, compound

https://huagongshe.com/reaction/552339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium hydrideHCID 24758—
ReactantHCID 67166149HCID 67166149—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67164696HCID 67164696—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 8-acetyl-3-(S)-benzyl-1,4,8-triazaspiro[4,5]decan-2-one (2.8 g, 9.7 mmol) in 20 mL of dry THF there was added sodium hydride (350 mg, 14.6 mmol) at 0° C. and under a blanket of nitrogen. Following stirring over a period of 1 h at 0° C., benzyl chloride (1.36 g, 10.7 mmol) was slowly added dropwise, and the mixture was allowed to warm up to RT and then heated under reflux over a period of 24 h. Following the addition of an aqueous saturated HCl solution (25 mL), the reaction mixture was isolated by filtration and the filtrate was extracted with EE (3×20 mL), and the combined organic phases were dried over Na2SO4. Following removal, by distillation, of the solvent, there was obtained the crude product as a yellow oil. Further purification was carried out by column chromatography. The product 8-acetyl-1,3-(S)-dibenzyl-1,4,8-triazaspiro[4,5]decan-2-one was obtained in a yield of 1.25 g (34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951815B2
Source datasetuspto-grants-2011_05
ORD IDord-13c124ec6e3a4bcc86721e483964c855
Source noteuspto-grants-2011_05