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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980285Generated: October 30, 2026

1,4-Dioxane hydrochloride → HCID 57048546, compound

https://huagongshe.com/reaction/1980285

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 57007444HCID 57007444—
ProductHCID 57048546HCID 5704854691.9%

Reaction Steps

20 ml of a 13% hydrogen chloride-dioxane solution are added to 1.2 g of tert.-butyl (4S)-1-benzyl-3-{(2S)-2-[N-((1S)-1-benzyloxycarbonyl-3-phenylpropyl)amino]propionyl}-2-oxo-imidazolidine-4-carboxylate, and the mixture is allowed to stand at room temperature overnight. The mixture is concentrated under reduced pressure to remove solvent. Ethyl acetate and water are added to the residue and the mixture is adjusted to pH 5 to 6 with an aqueous sodium bicarbonate solution. The ethyl acetate layer is collected therefrom, washed with a saturated sodium chloride solution and dried. The resultant solution is concentrated under reduced pressure to remove solvent, whereby 1.0 g of (4S)-1-benzyl-3-{(2S)-2-[N-((1S)-1-benzyloxycarbonyl-3-phenylpropyl)amino]propionyl}-2-oxo-imidazolidine-4-carboxylic acid is obtained as colorless viscous oil. Yield: 91.9%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04508727
Source datasetuspto-grants-1985_04
ORD IDord-55f776a20da74f8c895c8ceb2a1af5e3
Source noteuspto-grants-1985_04