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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924267Generated: November 2, 2026

1,4-Dioxane → HCID 53629169, compound

https://huagongshe.com/reaction/1924267

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantMorpholine, hydrochloride (1:1)HCID 197884—
Reactant4,4,4-TrifluorobutanalHCID 2777083—
ReactantGlyoxylic acid, monohydrateHCID 15620607—
SolventWaterHCID 962—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 53629169HCID 5362916981%

Reaction Steps

Glyoxylic acid monohydrate (2.43 g, 26.4 mmol), morpholine hydrochloride (3.59 g, 29 mmol) and dioxane (10.5 ml) are stirred together at room temperature. Water (14 ml) is added and the reaction mixture is stirred for a few minutes until it becomes homogeneous. 4,4,4-trifluorobutyraldehyde x99 (3.16 g, 25.1 mmol) is added and the mixture is stirred for 1 h at room temperature and under reflux conditions overnight. The mixture is diluted in tert-butylmethylether and washed with water. The aqueous phase is re-extracted with tert-butylmethylether. The organic extracts are combined, dried over magnesium sulphate, filtered and concentrated in vacuo to obtain 5-hydroxy-4-(2,2,2-trifluoroethyl)furan-2(5H)-one x100 as a yellow oil (3.76 g, 81%). The product is used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178533B2
Source datasetuspto-grants-2012_05
ORD IDord-f286ea5dcc4049dca8c50ddf32c4e5eb
Source noteuspto-grants-2012_05