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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474010Generated: October 29, 2026

Diisopropylamine → HCID 59420820, compound

https://huagongshe.com/reaction/474010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantEthyl propiolateHCID 12182—
Reactant3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59420820HCID 5942082064%

Reaction Conditions

Temperature0 °C

Reaction Steps

n-butyl lithium (1.17 mmol, 0.47 ml, 2.5 M) was added dropwise to a solution of diisopropylamine (130 mg, 1.29 mmol, 0.18 ml) in THF (8 ml) at −78° C. The solution was warmed to 0° C., stirred for 15 mins, and cooled back to −78° C. Ethyl propiolate (126 mg, 1.29 mmol, 0.13 ml) was added dropwise and the solution stirred for 1 hr at −78° C. A solution of tert-butyl 3-oxoazetidine-1-carboxylate (200 mg, 1.17° mmol) in THF (2 ml) was added dropwise, stirring continued for 30 mins, and the solution warmed to 0° C. and stirred for a further 15 mins. The reaction was quenched with Sat NH4Cl (20 ml) and extracted into ethyl acetate (20 ml), dried (Na2SO4), and concentrated to give a brown oil. The oil was purified by flash column chromatography eluting with 30% ethylacetate/hexanes to give the title compound as a colorless oil 0.20 g, 64%. 1H NMR (CDCl3, 400 MHz) 1.33 (3H, t), 1.48 (9H, s), 2.92 (1H, s), 4.04 (2H, d), 4.22-4.31 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637511B2
Source datasetuspto-grants-2014_01
ORD IDord-786e79386cfa4e68b3dce0edf39cb37a
Source noteuspto-grants-2014_01