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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565385Generated: October 29, 2026

HCID 18002561, compound → HCID 15411837, compound

https://huagongshe.com/reaction/565385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18002561HCID 18002561—
ReactantAluminium lithium hydrideHCID 21226445—
CatalystWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15411837HCID 15411837—
ProductHCID 18002536HCID 18002536—

Reaction Steps

To a stirred solution of (RS)-8-(acenaphthen-1-yl)-1-phenyl-1,8-diaza-spiro[4.5]decane-2,4-dione (0.67 g, 1.7 mmol) in THF (35 ml) was added at RT lithium aluminiumhydride (128 mg, 3.4 mmol) and the reaction mixture was boiled under reflux for 7 h. Water (20 drops) was added slowly at RT to the stirred solution and afterwards the reaction mixture was dried (Na2SO4) and filtered. The filtrate was evaporated and the crude product purified by column chromatography on silica gel (ethyl acetate/hexane 9:1) to yield (RS)-8-acenaphthen-1-yl-1-phenyl-1,8-diaza-spiro[4.5]decane (50 mg/see example 20) as a pale yellow oil and 8-(acenaphthen-1-yl)-1-phenyl-1,8-diaza-spiro[4.5]decan-4-ol (127 mg) as a pale brown foam, which while stirring was dissolved in 3N MeOH-HCl (0.5 ml) and treated with diethyl ether (15 ml). After 1 h the solid was filtered off to yield the desired product (128 mg, 55%) as a pale brown solid, m.p. 196° C. and MS: m/e=385.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172075B2
Source datasetuspto-grants-2001_01
ORD IDord-98cc00dfc9cd4e229b362921f17f2737
Source noteuspto-grants-2001_01