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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036047Generated: October 31, 2026

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

https://huagongshe.com/reaction/1036047

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-BuLi (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 solution 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 was 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 numberUS08546399B2
Source datasetuspto-grants-2013_10
ORD IDord-9e74f5046812479288793cbd80f934ba
Source noteuspto-grants-2013_10