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HRID 249263作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/249263

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物4-Propyl-1,2-benzenediolHCID 97638—
溶媒Diethyl EtherHCID 3283—
生成物6-n-Propyl-1,4-benzodioxine-2,3-dione monohydrateHCID 19760852165.3%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05214034
出典データセットuspto-grants-1993_05
ORD IDord-cadcf4ee32284d059c8c0d761c068ba4
出典メモuspto-grants-1993_05