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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428306Generated: October 29, 2026

Asparagusic acid → HCID 18358007, compound

https://huagongshe.com/reaction/428306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAsparagusic acidHCID 16682—
ReactantDiethyl cyanophosphonateHCID 76257—
ReactantMethyl 3-aminopropanoate hydrochlorideHCID 2734767—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18358007HCID 183580079.4%

Reaction Steps

The reaction was carried out as described in Example 97, but using 5 ml of a solution of 3.3 mmol of 1,2-dithiolane-4-carboxylic acid (prepared as described in Example 96) in anhydrous dimethylformamide, 5 ml of anhydrous tetrahydrofuran, 1.01 ml of torethylamine, 502 mg of β-alanine methyl ester hydrochloride and 0.55 ml of diethyl cyanophosphate. The solvent was removed from the reaction mixture by evaporation under reduced pressure, and water was added to the residue, after which it was extracted with ethyl acetate. The extraction solution was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The ethyl acetate was removed from the extraction solution by evaporation under reduced pressure, and the residue was subjected to silica gel column chromatography, using a 2:1 by volume mixture of ethyl acetate and hexane as the eluent. The solvent was removed from the eluate solution by evaporation under reduced pressure, and the residue was recrystallized from a 2:2 by volume mixture of ethyl acetate and hexane, to obtain 73 mg of the title compound as pale yellow crystals having an Rf value of 0.41 (silica gel thin layer chromatography; using a 2:1 by volume mixture of ethyl acetate and hexane as developing solvent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313164B1
Source datasetuspto-grants-2001_11
ORD IDord-68adbd173e544803b3b798faaeab5885
Source noteuspto-grants-2001_11