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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704003생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/704003

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물4-Propyl-1,2-benzenediolHCID 97638—
용매Diethyl EtherHCID 3283—
생성물6-n-Propyl-1,4-benzodioxine-2,3-dione monohydrateHCID 19760852165.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04985458
출처 데이터셋uspto-grants-1991_01
ORD IDord-963ea47ecc7940aaa873b5ea637ad2a9
출처 메모uspto-grants-1991_01