HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552348Generated: October 31, 2026
Benzyl Chloride → HCID 67166125, compound
https://huagongshe.com/reaction/552348
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 67166196 | HCID 67166196 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67166125 | HCID 67166125 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07951815B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-43c1098d47624f1087f82487fd13bbfe |
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| Source note | uspto-grants-2011_05 |
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