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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552348Generated: October 31, 2026

Benzyl Chloride → HCID 67166125, compound

https://huagongshe.com/reaction/552348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 67166196HCID 67166196—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67166125HCID 67166125—

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (1.26 g, 52.5 mmol) was added at RT to a solution of tert-butyl 3-(S)-benzyl-2-oxo-1,4,8-triazaspiro[4,5]decane-8-carboxylate (12.1 g, 35 mmol) in THF (250 ml). After stirring for 1 h at 0° C., benzyl chloride (4.9 g, 38.5 mmol) was added dropwise, and the mixture was allowed to warm to RT and heated for 60 h under reflux. Subsequently, benzyl chloride (2.4 g, 19 mmol) was again added and the mixture was heated under reflux for a further 16 h. The reaction mixture was treated with aqueous saturated NH4Cl solution (20 ml) and extracted with EA (3×50 ml). The combined organic phase was dried over Na2SO4, filtered and the solvent was distilled off. Workup was carried out by means of column chromatography and afforded tert-butyl-1,3-(S)-dibenzyl-2-oxo-1,4,8-triazaspiro[4,5]decane-8-carboxylate in a yield of 13.5 g (88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951815B2
Source datasetuspto-grants-2011_05
ORD IDord-43c1098d47624f1087f82487fd13bbfe
Source noteuspto-grants-2011_05