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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969408Generated: October 30, 2026

Water → 5-((R)-alpha-methylbenzyl)-7-hydroxy-5-azaspiro[2.4]heptane

https://huagongshe.com/reaction/1969408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 11775986HCID 11775986—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product5-((R)-alpha-methylbenzyl)-7-hydroxy-5-azaspiro[2.4]heptaneHCID 2285047185%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of LiAlH4 (0.995 g, 26.2 mmol) in THF (40 mL) was added a solution of 5-((R)-α-methylbenzyl)-4,7-dioxo-5-azaspiro[2.4]heptane (3.0 g, 13.1 mmol) in THF (10 mL) at 0° C. The reaction mixture was stirred at 0° C. for 2 hrs, then warmed up to 50° C. and continued to stir for 6 hrs. The reaction mixture was then cooled to 0° C. and ethyl acetate (10 mL) and water (10 mL) were added. The suspension was filtered and the filtrate was concentrated in vacuo. The residue was purified by a silica gel column chromatography (1:3 (v/v) 2-butanol/n-hexane) to afford the title compound as colorless oil (2.4 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426585B2
Source datasetuspto-grants-2013_04
ORD IDord-ce98375d32954819979d9c801804d72f
Source noteuspto-grants-2013_04