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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1460193생성일: 2026년 10월 26일

Triethylamine → Methyl 4-(2,3,4-trimethoxybenzoyl)-1-piperazinecarbodithioate

https://huagongshe.com/reaction/1460193

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,3,4-Trimethoxybenzoic acidHCID 11308—
반응물Thionyl ChlorideHCID 24386—
반응물Methyl piperazine-1-carbodithioateHCID 21278808—
용매DichloromethaneHCID 6344—
생성물Methyl 4-(2,3,4-trimethoxybenzoyl)-1-piperazinecarbodithioateHCID 1938849051.6%

반응 단계

In a nitrogen atmosphere, 10 ml (138 mmol.) of thionyl chloride was added to 1.00 g (4.71 mmol.) of 2,3,4-trimethoxybenzoic acid. The mixture was refluxed under heating for 2 hours. The solvent was distilled off under reduced pressure. To the residue was added 10 ml of dry benzene, and the mixture was placed under reduced pressure to distill off benzene. This procedure was repeated once. To the residue was dropwise added at room temperature a solution of 0.88 g (4.74 mmol., purity 95%) of methyl 1-piperazinecarbodithioate in 12 ml of dichloromethane. In the course of the addition, 0.48 g (4.74 mmol.) of triethylamine was added to the mixture. The resulting mixture was then stirred overnight. The reaction mixture was washed successively with 1-N hydrochloric acid and a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and placed under pressure to distill off the solvent. The residue was crystallized from acetone. The crystals were collected by filtration. The filtrate was concentrated, and additional crystals were further precipitated from the concentrated filtrate by addition of a small amount of ethanol. These crystalline portions were combined to give 0.90 g of the desired compound as a white crystalline product, m.p. 149°-150° C. (decomp.), yield 51.6%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05070089
출처 데이터셋uspto-grants-1991_12
ORD IDord-eb249bbefe74479fae360de952c3629f
출처 메모uspto-grants-1991_12