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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721336Generated: November 1, 2026

1,4-Dioxane → HCID 10379793, compound

https://huagongshe.com/reaction/1721336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 54284844HCID 54284844—
SolventWaterHCID 962—
ProductHCID 10379793HCID 1037979359.9%

Reaction Steps

A stirred solution of 6.0 g of 4-chloro-β-(dimethylamino)-α-(3-methyl-2-thienoyl)-2-nitrosty rene, 50 ml of 1,4-dioxane and 10 ml of water was refluxed for 16 hr and allowed to cool. The cooled solution was concentrated, and the residue was partitioned between dichloromethane and water. The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated. A stirred solution of the residue, dioxane and water was refluxed overnight and was worked-up as above. The residue was purified by preparative HPLC (Waters Associates Prep LC./Model 500, silica gel, sample applied in dichloromethane (20 ml), eluted with dichloromethane, 200 ml/min flow rate, Gow Mac Model 80-800 UV detector). The appropriate fractions were concentrated and the residue was recrystallized from 95% ethanol to give 3.03 g of product, mp 105°-107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05510346
Source datasetuspto-grants-1996_04
ORD IDord-32f974bdeef14d48ba422988b7f16432
Source noteuspto-grants-1996_04