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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393639Generated: October 30, 2026

1,4-Dioxane → HCID 20038701, compound

https://huagongshe.com/reaction/1393639

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantAzane;hydrateHCID 12896473—
ReactantHCID 23091968HCID 23091968—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20038701HCID 2003870181%

Reaction Steps

3-t-Butyl thiazolidine-3,4-dicarboxylate (2.0 g) was dissolved in tetrahydrofuran (10 ml), and N,N′-carbonyl diimidazole (1.4 g) was added thereto with ice-cooling. The mixture was warmed to room temperature and stirred for 6 hours. 1,4-Dioxane (10 ml) was added thereto, and the mixture was added dropwise to 28% ammonia water (40 ml) cooled on an ice bath. The mixture was warmed to room temperature and stirred for 20 hours. The reaction solution was extracted with ethyl acetate (60 ml). The organic phase was washed with a saturated saline solution and dried over sodium sulfate anhydrous. The product was concentrated under reduced pressure to give t-butyl 4-carbamoylthiazolidine-3-carboxylate (1.6 g, Y.:81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345180B2
Source datasetuspto-grants-2008_03
ORD IDord-f8213438ade54b82b880066a0d1e47dd
Source noteuspto-grants-2008_03