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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552349Generated: October 29, 2026

Benzyl Chloride → tert-butyl 1-benzyl-3-(S)-(2-methylsulfanylethyl)-2-oxo-1,4,8-triazaspiro[4,5]decane-8-carboxylate

https://huagongshe.com/reaction/552349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl 3-(S)-(2-methylsulfanylethyl)-2-oxo-1,4,8-triazaspiro[4,5]decane-8-carboxylateHCID 67166130—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 1-benzyl-3-(S)-(2-methylsulfanylethyl)-2-oxo-1,4,8-triazaspiro[4,5]decane-8-carboxylateHCID 67165908—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of tert-butyl 3-(S)-(2-methylsulfanylethyl)-2-oxo-1,4,8-triazaspiro-[4,5]decane-8-carboxylate (4.4 g, 13.4 mmol) in THF (72 ml) was added dropwise at 0° C. to a suspension of NaH (385 mg, 16.0 mmol) in THF (60 ml). After stirring for 1 h at 0° C., benzyl chloride (2.0 g, 16.0 mmol) was added dropwise, and the mixture was allowed to warm to RT and was heated for 68 h under reflux. The reaction mixture was treated with aqueous saturated NH4Cl solution (20 ml), the organic phase was separated off and the aqueous phase was extracted with EA (3×50 ml). The combined organic phase was dried over Na2SO4, filtered and the solvent was distilled off. The workup was carried out by means of column chromatography and afforded tert-butyl 1-benzyl-3-(S)-(2-methylsulfanylethyl)-2-oxo-1,4,8-triazaspiro[4,5]decane-8-carboxylate in a yield of 1.6 g (30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951815B2
Source datasetuspto-grants-2011_05
ORD IDord-ebe92862ea94440fbc7f5bd5953b7bfa
Source noteuspto-grants-2011_05