Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573203Generated: October 29, 2026

Diisopropylamine → Diethyl 1,4-dioxaspiro[4.5]decane-8,8-dicarboxylate

https://huagongshe.com/reaction/573203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantEthyl chloroformateHCID 10928—
ReactantEthyl 1,4-dioxaspiro(4.5)decane-8-carboxylateHCID 10488810—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductDiethyl 1,4-dioxaspiro[4.5]decane-8,8-dicarboxylateHCID 67170753—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 500 mL round-bottomed flask was charged with diisopropylamine (16 mL) and tetrahydrofuran (311 mL). The solution was cooled to −78° C. under N2 and n-butyllithium (2.5 M in hexanes, 44.8 mL)) was added. The reaction was stirred for 30 minutes at −78° C. and ethyl 1,4-dioxaspiro[4.5]decane-8-carboxylate (20 g) was added as a tetrahydrofuran solution (ca. 10 mL). The mixture was stirred at −78° C. for 1 hour and ethyl chloroformate (9 mL) was added neat. After stirring at −78° C. for 10 minutes, the reaction was warmed to room temperature over 2 hours. The reaction was quenched with saturated aqueous NH4Cl and diluted with diethyl ether. The layers were separated, the aqueous layer was extracted with diethyl ether and the combined organics were dried (Na2SO4), filtered and concentrated by rotary evaporation. The residue was purified by regular phase flash column chromatography (Analogix, 0-65% hexanes/ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029404B2
Source datasetuspto-grants-2015_05
ORD IDord-2c4e928ba505439ebb866e6a8a9dde75
Source noteuspto-grants-2015_05