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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249263Generated: October 25, 2026

Triethylamine → 6-n-Propyl-1,4-benzodioxine-2,3-dione monohydrate

https://huagongshe.com/reaction/249263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant4-Propyl-1,2-benzenediolHCID 97638—
SolventDiethyl EtherHCID 3283—
Product6-n-Propyl-1,4-benzodioxine-2,3-dione monohydrateHCID 19760852165.3%

Reaction Steps

A mixture of 3.81 g (25 mM) of 4-n-propylcatechol, 5.06 g (50 mM) of triethylamine and 50 ml of dry ether was cooled in an ice water bath so as to maintain the temperature at 5° C. or below. The mixture was added dropwise over 1.5 hours under stirring with a solution of 3.50 g (28 mM) of oxalyl chloride in 10 ml of dry ether. After completing the dropwise addition, the temperature of the reaction mixture was gradually raised to the room temperature and then aging was conducted for an hour. The resultant mixture was heated under reflux for 3 hours in order to complete the aging. The separated crystals of triethyl ammonium chloride was filtered. After thoroughly washing the crystals with ether, the ether solution was collected and dried with anhydrous sodium sulfate. After distilling off ether, the reaction product was recrystallized from a solvent mixture of carbontetrachloride and petroleum benzine to obtain 4.64 g (22.5 mM) of 6-n-propyl-1,4-benzodioxine-2,3-dione monohydrate as colorless crystals having a melting point of 99°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05214034
Source datasetuspto-grants-1993_05
ORD IDord-cadcf4ee32284d059c8c0d761c068ba4
Source noteuspto-grants-1993_05