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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747017Generated: October 29, 2026

Tetrahydrofuran → Benzyl 4-(acetyloxy)-3,3-dimethyl-1-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/reaction/747017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-(acetyloxy)-2-methylPropanalHCID 12735633—
Reactant1-Benzyl 4-ethyl piperidine-1,4-dicarboxylateHCID 15289672—
ProductBenzyl 4-(acetyloxy)-3,3-dimethyl-1-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 69148927—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 1-benzyl 4-ethyl piperidine-1,4-dicarboxylate (2.35 g) was dissolved in tetrahydrofuran (30 mL) and was cooled to −78° C. Lithium bis(trimethylsilyl)amide (9 mL, 1M) was added dropwise under nitrogen and the solution was stirred for 30 min at −20° C. The solution was re-cooled to −78° C. and 1,1-dimethyl-2-oxoethyl acetate (1.17 g) in tetrahydrofuran (5 mL) was added and the mixture was stirred for 30 min. The mixture was quenched (NaHCO3, 30 mL) and the mixture was extracted with ethyl acetate (2×50 mL). The extracts were combined, washed with brine, dried (MgSO4) and were concentrated in vacuo. The crude product was purified by chromatography on silica using 25-75% ethyl acetate in iso-hexane as eluant to afford the product (1.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393858B2
Source datasetuspto-grants-2008_07
ORD IDord-c64c67d4640f4af8913bfca29e5defdd
Source noteuspto-grants-2008_07