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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1753723생성일: 2026년 10월 24일

Cyanamide → HCID 89766894, 화합물

https://huagongshe.com/ko/reaction/1753723

반응식

참여 물질

역할이름HCID투입량
반응물CyanamideHCID 9864—
반응물N-bromobutanimideHCID 67184—
반응물Sodium permanganate monohydrateHCID 516876—
반응물Sodium BisulfateHCID 516919—
반응물Potassium tert-butoxideHCID 23665647—
반응물2-Methoxy-3-methylthio-4-(trifluoromethyl)benzoic acidHCID 66957907—
용매MethanolHCID 887—
생성물HCID 89766894HCID 8976689426.9%

반응 단계

3.71 g (33.1 mmol) of potassium tert-butoxide were added to a solution of 4.00 g (15.0 mmol) of 2-methoxy-3-(methylsulfanyl)-4-(trifluoromethyl)benzoic acid in 250 ml of methanol. The mixture was stirred for 10 minutes, and 1.07 g (25.5 mmol) of cyanamide and 4.81 g (27.0 mmol) of N-bromosuccinimide were then added in succession. The contents were then stirred at RT for 2 h. The mixture was then freed from the solvent on a rotary evaporator and the residue was taken up in a mixture of in each case 120 ml of acetonitrile and water. 7.21 g (45.1 mmol) of sodium permanganate monohydrate were added, and the mixture was stirred at RT for one week. During this week, both after one day and after a further day, in each case 3.6 g (22.5 mmol) of sodium permanganate monohydrate were added. For work-up, a 10% by weight strength solution of sodium bisulfate was added. On a rotary evaporator, at a temperature of at most 30° C., the solvent was substantially removed. The residue was cooled in an ice bath and then acidified with 1M hydrochloric acid. The mixture was extracted three times with ice-cold dichloromethane. The combined organic phases were freed from the solvent on a rotary evaporator and the residue was purified chromatographically, which gave 1.30 g of product of a purity of 80% by weight.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09167819B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-331770813eb748e7a0f3a5ada4bd4a81
출처 메모uspto-grants-2015_10