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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665206Generated: October 31, 2026

Tetrahydrofuran → HCID 131729236, compound

https://huagongshe.com/reaction/1665206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantSodium chloride; waterHCID 57417360—
ReactantHCID 86634961HCID 86634961—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 131729236HCID 131729236—

Reaction Steps

0.32 g of (1R)-trans-3-[(E)-3-methoxyimino-2-methyl-1-propenyl]-2,2-dimethylcyclopropanecarboxylic acid, catalytic amount of 4-dimethylaminopyridine and 5 ml of anhydrous tetrahydrofuran was added 0.30 g of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and the mixture was stirred at room temperature overnight. Thereafter, saturated brine was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, then, filtrated, and the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.34 g of 2,5-dioxo-3-(2-propynyl)imidazolidin-1-ylmethyl (1R)-trans-3-[(E)-3-methoxyimino-2-methyl-1-propenyl]-2,2-dimethylcyclopropanecarboxylate (hereinafter, referred to as the present compound (1)) represented by the formula (1):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039499B2
Source datasetuspto-grants-2011_10
ORD IDord-fcd6405489354f37918e599f96e486f4
Source noteuspto-grants-2011_10