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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721810Generated: November 2, 2026

1,1'-Carbonyldiimidazole → HCID 54534973, compound

https://huagongshe.com/reaction/1721810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3-Methyl-5-isoxazolecarboxylic acidHCID 76947—
ReactantL-Alanine, ethyl ester, hydrochloride (1:1)HCID 2724356—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54534973HCID 54534973—

Reaction Steps

8.2 g of 1,1'-carbonyldiimidazole (CDI) was added to a mixture of 6.35 g of 1B and 75 ml of dry tetrahydrofuran (THF) and the mixture was stirred for 2 hours at room temperature. Then 7.5 g of alanine ethyl ester hydrochloride was added, the mixture was stirred overnight, filtered, and the filtrate was stripped of solvent. The residue was dissolved in 100 ml of a 9:1 v:v mixture of methylene chloride and ethyl acetate, the solution was filtered through silica gel, the gel was washed with 900 ml of the same solvent, then the combined filtrate and washings was stripped of solvent. The residue was a yellow oil that crystallized on standing. The crystals were washed with pentane and dried, to give N-(5-methyl-3-isoxazolylcarbonyl)alanine ethyl ester (1C), as a solid, m.p.: 65°-66° C. 1C was converted to the corresponding acid (1D, a solid, m.p.: 148°-150° C.) in the manner that 1A was converted to 1B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04853027
Source datasetuspto-grants-1989_08
ORD IDord-d9fe60ce89734c6b8c6ac535663d4bd5
Source noteuspto-grants-1989_08