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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011599Generated: October 31, 2026

Dichloromethane → (s)-tert-Butyl 2-cyclopropyl-3,5-dioxopyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1011599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
Reactant2-(Tert-butoxycarbonylamino)-2-cyclopropylacetic acidHCID 22492146—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
Product(s)-tert-Butyl 2-cyclopropyl-3,5-dioxopyrrolidine-1-carboxylateHCID 57659759—

Reaction Steps

2-(tert-Butoxycarbonylamino)-2-cyclopropylacetic acid (13) (5.47 g, 25.4 mmol), Meldrum's acid (14) (4.02 g, 27.9 mmol), and DMAP (4.34 g, 35.56 mmol) were added to CH2Cl2 (100 mL) under nitrogen at 0° C. After 30 minutes EDAC (6.81 g, 35.56 mmol) was added. The reaction was stirred 16 hr at rt and poured into EtOAc (300 mL), washed with brine (200 ml), 5% citric acid (300 mL), and again brine (200 mL). The organic phase was then refluxed for 1 hr. The mixture was evaporated to give (S)-tert-butyl 2-cyclopropyl-3,5-dioxopyrrolidine-1-carboxylate (15) a yellow oil (4.0 g, 69%) that was taken into the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977368B2
Source datasetuspto-grants-2011_07
ORD IDord-c2d6b44d8ea54d2386b2d38ec96928f7
Source noteuspto-grants-2011_07