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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036018Generated: October 26, 2026

3-Ethoxycyclohex-2-ene-1-one → Spiro[2.5]octan-5-one

https://huagongshe.com/reaction/1036018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Ethoxycyclohex-2-ene-1-oneHCID 79216—
ReactantHCID 178418443HCID 178418443—
CatalystTitanium isopropoxideHCID 11026—
SolventDiethyl EtherHCID 3283—
ProductSpiro[2.5]octan-5-oneHCID 12153480—

Reaction Steps

To a solution of 3-ethoxycyclohex-2-enone (48.1 mL) in ether (1000 mL) was added titanium(IV) isopropoxide (110 mL) followed by addition of ethylmagnesium bromide (357 mL) at ambient temperature. The reaction mixture was stirred for 2 hours at ambient temperature and was then quenched with water (500 mL). The organic layer was separated (decanted) and the water layer was extracted with ether (3×300 mL). The combined extracts were partially concentrated to approximately 300 mL. p-Toluenesulfonic acid monohydrate (3.0 g) was added and the reaction mixture was stirred overnight at ambient temperature. The reaction mixture was then washed with saturated aqueous NaHCO3 solution, dried (MgSO4), filtered and concentrated. The concentrate was purified by fractional distillation (1st fraction b.p. 27° C. at 23 torr (not product), 2nd fraction (product) b.p. 75° C. at 8 torr).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546399B2
Source datasetuspto-grants-2013_10
ORD IDord-f783107470a049629df258cbc30e380a
Source noteuspto-grants-2013_10